UPDATE - Protein Allele ID & Protein Sequence HGVS Requests Partially Restored
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
Linked Data
MyVariant Identifiers:
chr11:g.17429993C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.17408446C>T , CM000673.2:g.17408446C>T | GRCh38 |
| NC_000011.9:g.17429993C>T , CM000673.1:g.17429993C>T | GRCh37 |
| NC_000011.8:g.17386569C>T | NCBI36 |
| NG_008867.1:g.73457G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000524561.2:n.2435G>A | ||
| ENST00000529967.6:n.1025G>A | ||
| ENST00000532220.2:n.498G>A | ||
| ENST00000642611.2:n.2835G>A | ||
| ENST00000682051.1:n.2782G>A | ||
| ENST00000682110.1:n.2835G>A | ||
| ENST00000682140.1:c.2763G>A | ENSP00000507829.1:p.Gln921= | |
| ENST00000682185.1:n.4071G>A | ||
| ENST00000682204.1:c.*904G>A | ENSP00000507094.1:n.*904G>A | |
| ENST00000682215.1:n.2832G>A | ||
| ENST00000682288.1:c.*1197G>A | ENSP00000507506.1:n.*1197G>A | |
| ENST00000682442.1:n.2956G>A | ||
| ENST00000682528.1:n.2832G>A | ||
| ENST00000682673.1:n.2779G>A | ||
| ENST00000682805.1:n.2832G>A | ||
| ENST00000682965.1:c.2763G>A | ENSP00000508229.1:p.Gln921= | |
| ENST00000683093.1:n.2934G>A | ||
| ENST00000683136.1:c.2763G>A | ENSP00000507768.1:p.Gln921= | |
| ENST00000683153.1:n.2991G>A | ||
| ENST00000683365.1:n.2937G>A | ||
| ENST00000683377.1:n.2835G>A | ||
| ENST00000683456.1:c.2766G>A | ENSP00000508318.1:p.Gln922= | |
| ENST00000683522.1:n.2835G>A | ||
| ENST00000683562.1:c.*935G>A | ENSP00000508265.1:n.*935G>A | |
| ENST00000683693.1:n.2832G>A | ||
| ENST00000683725.1:c.2766G>A | ENSP00000507496.1:p.Gln922= | |
| ENST00000684010.1:n.2750G>A | ||
| ENST00000684157.1:n.2835G>A | ||
| ENST00000684253.1:n.2738G>A | ||
| ENST00000684288.1:c.*938G>A | ENSP00000507143.1:n.*938G>A | |
| ENST00000684313.1:n.2267G>A | ||
| ENST00000684332.1:n.2908G>A | ||
| ENST00000684371.1:n.2941G>A | ||
| ENST00000684404.1:n.2832G>A | ||
| ENST00000684442.1:n.2835G>A | ||
| ENST00000684555.1:c.*978G>A | ENSP00000507705.1:n.*978G>A | |
| ENST00000684571.1:c.2607G>A | ENSP00000506935.1:p.Gln869= | |
| ENST00000684593.1:c.*2471G>A | ENSP00000507005.1:n.*2471G>A | |
| ENST00000684711.1:c.*1162G>A | ENSP00000506841.1:n.*1162G>A | |
| ENST00000302539.9:c.2769G>A | ENSP00000303960.4:p.Gln923= | |
| ENST00000389817.8:c.2766G>A MANE Select | ENSP00000374467.4:p.Gln922= | |
| ENST00000642271.1:c.2763G>A | ENSP00000493749.1:p.Gln921= | |
| ENST00000642579.1:c.850G>A | ||
| ENST00000642611.1:n.2720G>A | ||
| ENST00000642902.1:c.2601G>A | ||
| ENST00000643260.1:c.2766G>A | ENSP00000494450.1:p.Gln922= | |
| ENST00000643562.1:c.*742G>A | ENSP00000496124.1:n.*742G>A | |
| ENST00000643925.1:c.810G>A | ||
| ENST00000644447.1:c.1122G>A | ENSP00000496282.1:p.Gln374= | |
| ENST00000644472.1:c.*1127G>A | ENSP00000495378.1:n.*1127G>A | |
| ENST00000644484.1:c.*975G>A | ENSP00000493558.1:n.*975G>A | |
| ENST00000644542.1:c.*2471G>A | ENSP00000495532.1:n.*2471G>A | |
| ENST00000644675.1:c.*938G>A | ENSP00000494567.1:n.*938G>A | |
| ENST00000644757.1:c.*1071G>A | ENSP00000495085.1:n.*1071G>A | |
| ENST00000644772.1:c.2832G>A | ENSP00000494321.1:p.Gln944= | |
| ENST00000645076.1:c.2018G>A | ||
| ENST00000645744.1:c.*1130G>A | ENSP00000494564.1:n.*1130G>A | |
| ENST00000645760.1:c.3041G>A | ||
| ENST00000645884.1:c.2766G>A | ENSP00000495516.1:p.Gln922= | |
| ENST00000646003.1:c.*822G>A | ENSP00000495259.1:n.*822G>A | |
| ENST00000646207.1:c.*1130G>A | ENSP00000495025.1:n.*1130G>A | |
| ENST00000646276.1:c.*1039G>A | ENSP00000496070.1:n.*1039G>A | |
| ENST00000646592.1:c.1992G>A | ||
| ENST00000646902.1:c.2763G>A | ENSP00000494101.1:p.Gln921= | |
| ENST00000646993.1:c.*1162G>A | ENSP00000493720.1:n.*1162G>A | |
| ENST00000647013.1:c.2772G>A | ENSP00000496741.1:n.2772G>A | |
| ENST00000647015.1:c.2517G>A | ENSP00000495389.1:p.Gln839= | |
| ENST00000647086.1:c.*2496G>A | ENSP00000493677.1:n.*2496G>A | |
| ENST00000647158.1:c.*907G>A | ENSP00000495744.1:n.*907G>A | |
| ENST00000302539.8:c.2769G>A | ENSP00000303960.4:p.Gln923= | |
| ENST00000389817.7:c.2766G>A | ENSP00000374467.3:p.Gln922= | |
| ENST00000526921.5:n.450G>A | ||
| ENST00000527905.5:c.2736G>A | ENSP00000431653.1:p.Gln912= | |
| ENST00000529967.5:n.435G>A | ||
| NM_000352.4:c.2766G>A | NP_000343.2:p.Gln922= | |
| NM_001287174.1:c.2769G>A | NP_001274103.1:p.Gln923= | |
| XM_011520331.1:c.2766G>A | XP_011518633.1:p.Gln922= | |
| XM_011520332.1:c.2769G>A | XP_011518634.1:p.Gln923= | |
| XM_011520333.1:c.1266G>A | XP_011518635.1:p.Gln422= | |
| XM_011520334.1:c.2769G>A | XP_011518636.1:p.Gln923= | |
| XR_930890.1:n.2832G>A | ||
| XR_930891.1:n.2832G>A | ||
| XR_930892.1:n.2832G>A | ||
| XR_930893.1:n.2829G>A | ||
| NM_001351295.1:c.2832G>A | NP_001338224.1:p.Gln944= | |
| NM_001351296.1:c.2766G>A | NP_001338225.1:p.Gln922= | |
| NM_001351297.1:c.2763G>A | NP_001338226.1:p.Gln921= | |
| NR_147094.1:n.2835G>A | ||
| XM_017018197.2:c.2835G>A | XP_016873686.1:p.Gln945= | |
| XM_017018199.1:c.2832G>A | XP_016873688.1:p.Gln944= | |
| XM_017018201.2:c.2835G>A | XP_016873690.1:p.Gln945= | |
| XM_017018202.1:c.1332G>A | XP_016873691.1:p.Gln444= | |
| XM_017018204.1:c.723G>A | XP_016873693.1:p.Gln241= | |
| XM_024448668.1:c.1134G>A | XP_024304436.1:p.Gln378= | |
| XR_001747945.2:n.2907G>A | ||
| XR_001747946.2:n.2838G>A | ||
| XR_002957189.1:n.2907G>A | ||
| NM_000352.6:c.2766G>A MANE Select | NP_000343.2:p.Gln922= | |
| NM_001287174.2:c.2769G>A | NP_001274103.1:p.Gln923= | |
| NM_001351295.2:c.2832G>A | NP_001338224.1:p.Gln944= | |
| NM_001351296.2:c.2766G>A | NP_001338225.1:p.Gln922= | |
| NM_001351297.2:c.2763G>A | NP_001338226.1:p.Gln921= | |
| NR_147094.2:n.2835G>A | ||
| NM_001287174.3:c.2769G>A | NP_001274103.1:p.Gln923= |