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
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.152140045A>C , CM000668.2:g.152140045A>C | GRCh38 |
| NC_000006.11:g.152461180A>C , CM000668.1:g.152461180A>C | GRCh37 |
| NC_000006.10:g.152502873A>C | NCBI36 |
| NG_012855.1:g.502355T>G | |
| NG_012855.2:g.502355T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000354674.5:c.1897T>G MANE Plus Clinical | ENSP00000346701.4:p.Trp633Gly | |
| ENST00000367255.10:c.25363T>G MANE Select | ENSP00000356224.5:p.Trp8455Gly | |
| ENST00000423061.6:c.25219T>G | ENSP00000396024.1:p.Trp8407Gly | |
| ENST00000672154.1:c.765T>G | ||
| ENST00000672169.1:c.1098T>G | ||
| ENST00000673173.1:c.1007T>G | ||
| ENST00000673451.1:c.1135T>G | ENSP00000500189.1:p.Trp379Gly | |
| ENST00000341594.9:c.24148T>G | ENSP00000341887.6:p.Trp8050Gly | |
| ENST00000347037.9:n.2111T>G | ||
| ENST00000354674.4:c.1897T>G | ENSP00000346701.4:p.Trp633Gly | |
| ENST00000367251.7:c.4198T>G | ENSP00000356220.3:p.Trp1400Gly | |
| ENST00000367255.9:c.25363T>G | ENSP00000356224.5:p.Trp8455Gly | |
| ENST00000367256.9:n.9055T>G | ||
| ENST00000367257.8:c.3301T>G | ENSP00000356226.4:p.Trp1101Gly | |
| ENST00000409694.6:n.8947T>G | ||
| ENST00000423061.5:c.25219T>G | ENSP00000396024.1:p.Trp8407Gly | |
| ENST00000460912.6:n.1977T>G | ||
| ENST00000478916.5:n.4385T>G | ||
| ENST00000536990.5:n.2200T>G | ||
| ENST00000539504.5:c.1828T>G | ENSP00000441052.1:p.Trp610Gly | |
| NM_033071.3:c.25219T>G | NP_149062.1:p.Trp8407Gly | |
| NM_182961.3:c.25363T>G | NP_892006.3:p.Trp8455Gly | |
| XM_006715407.1:c.25468T>G | XP_006715470.1:p.Trp8490Gly | |
| XM_006715408.1:c.25456T>G | XP_006715471.1:p.Trp8486Gly | |
| XM_006715409.1:c.25447T>G | XP_006715472.1:p.Trp8483Gly | |
| XM_006715410.1:c.25468T>G | XP_006715473.1:p.Trp8490Gly | |
| XM_006715411.1:c.25417T>G | XP_006715474.1:p.Trp8473Gly | |
| XM_006715412.1:c.25453T>G | XP_006715475.1:p.Trp8485Gly | |
| XM_006715413.1:c.25399T>G | XP_006715476.1:p.Trp8467Gly | |
| XM_006715414.1:c.25396T>G | XP_006715477.1:p.Trp8466Gly | |
| XM_006715415.1:c.25399T>G | XP_006715478.1:p.Trp8467Gly | |
| XM_006715416.1:c.25384T>G | XP_006715479.1:p.Trp8462Gly | |
| XM_006715417.1:c.25327T>G | XP_006715480.1:p.Trp8443Gly | |
| XM_006715420.1:c.25315T>G | XP_006715483.1:p.Trp8439Gly | |
| XM_006715421.1:c.25312T>G | XP_006715484.1:p.Trp8438Gly | |
| XM_006715422.1:c.25309T>G | XP_006715485.1:p.Trp8437Gly | |
| XM_006715423.1:c.25468T>G | XP_006715486.1:p.Trp8490Gly | |
| XM_006715424.1:c.25468T>G | XP_006715487.1:p.Trp8490Gly | |
| XM_006715425.1:c.25399T>G | XP_006715488.1:p.Trp8467Gly | |
| XM_011535641.1:c.25465T>G | XP_011533943.1:p.Trp8489Gly | |
| XM_011535642.1:c.25453T>G | XP_011533944.1:p.Trp8485Gly | |
| XM_011535643.1:c.25303T>G | XP_011533945.1:p.Trp8435Gly | |
| XM_011535644.1:c.23743T>G | XP_011533946.1:p.Trp7915Gly | |
| XM_011535645.1:c.23236T>G | XP_011533947.1:p.Trp7746Gly | |
| XM_011535647.1:c.18703T>G | XP_011533949.1:p.Trp6235Gly | |
| NM_001347701.1:c.1969T>G | NP_001334630.1:p.Trp657Gly | |
| NM_001347702.1:c.1897T>G | NP_001334631.1:p.Trp633Gly | |
| XM_006715408.2:c.25456T>G | XP_006715471.1:p.Trp8486Gly | |
| XM_006715410.2:c.25468T>G | XP_006715473.1:p.Trp8490Gly | |
| XM_006715412.2:c.25453T>G | XP_006715475.1:p.Trp8485Gly | |
| XM_006715413.2:c.25399T>G | XP_006715476.1:p.Trp8467Gly | |
| XM_006715415.2:c.25399T>G | XP_006715478.1:p.Trp8467Gly | |
| XM_006715416.2:c.25384T>G | XP_006715479.1:p.Trp8462Gly | |
| XM_006715417.2:c.25327T>G | XP_006715480.1:p.Trp8443Gly | |
| XM_006715420.2:c.25315T>G | XP_006715483.1:p.Trp8439Gly | |
| XM_006715421.2:c.25312T>G | XP_006715484.1:p.Trp8438Gly | |
| XM_006715423.2:c.25468T>G | XP_006715486.1:p.Trp8490Gly | |
| XM_006715424.2:c.25468T>G | XP_006715487.1:p.Trp8490Gly | |
| XM_006715425.2:c.25399T>G | XP_006715488.1:p.Trp8467Gly | |
| XM_011535641.2:c.25465T>G | XP_011533943.1:p.Trp8489Gly | |
| XM_011535642.2:c.25453T>G | XP_011533944.1:p.Trp8485Gly | |
| XM_011535645.2:c.23236T>G | XP_011533947.1:p.Trp7746Gly | |
| XM_017010608.1:c.25468T>G | XP_016866097.1:p.Trp8490Gly | |
| XM_017010609.1:c.25468T>G | XP_016866098.1:p.Trp8490Gly | |
| XM_017010610.1:c.25447T>G | XP_016866099.1:p.Trp8483Gly | |
| XM_017010611.2:c.25441T>G | XP_016866100.1:p.Trp8481Gly | |
| XM_017010612.1:c.25390T>G | XP_016866101.1:p.Trp8464Gly | |
| XM_017010613.1:c.25396T>G | XP_016866102.1:p.Trp8466Gly | |
| XM_017010614.1:c.25312T>G | XP_016866103.1:p.Trp8438Gly | |
| XM_017010615.1:c.25243T>G | XP_016866104.1:p.Trp8415Gly | |
| XM_017010616.1:c.25399T>G | XP_016866105.1:p.Trp8467Gly | |
| XM_017010617.1:c.25396T>G | XP_016866106.1:p.Trp8466Gly | |
| XM_017010618.1:c.25384T>G | XP_016866107.1:p.Trp8462Gly | |
| XM_017010619.1:c.23743T>G | XP_016866108.1:p.Trp7915Gly | |
| NM_182961.4:c.25363T>G MANE Select | NP_892006.3:p.Trp8455Gly | |
| NM_001347701.2:c.1969T>G | NP_001334630.1:p.Trp657Gly | |
| NM_001347702.2:c.1897T>G MANE Plus Clinical | NP_001334631.1:p.Trp633Gly | |
| NM_033071.5:c.25219T>G | NP_149062.2:p.Trp8407Gly |