Linked Data
ClinVar Variation Id:
466132
dbSNP Id:
rs762641110
ExAC:
9:135771767 A / G
gnomAD v2:
9-135771767-A-G
gnomAD v3:
9-132896380-A-G
gnomAD v4:
9-132896380-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.132896380A>G , CM000671.2:g.132896380A>G | GRCh38 |
| NC_000009.11:g.135771767A>G , CM000671.1:g.135771767A>G | GRCh37 |
| NC_000009.10:g.134761588A>G | NCBI36 |
| NG_012386.1:g.53254T>C , LRG_486:g.53254T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000475903.7:c.3347T>C | ENSP00000496126.2:p.Leu1116Pro | |
| ENST00000490179.4:c.3350T>C | ENSP00000495533.2:p.Leu1117Pro | |
| ENST00000642261.2:c.*1206T>C | ENSP00000494743.2:n.*1206T>C | |
| ENST00000643275.2:c.*1290T>C | ENSP00000495598.2:n.*1290T>C | |
| ENST00000643362.2:c.2963T>C | ENSP00000496398.2:p.Leu988Pro | |
| ENST00000643625.2:c.*1092T>C | ENSP00000495546.2:n.*1092T>C | |
| ENST00000643691.2:c.2987T>C | ENSP00000494916.2:p.Leu996Pro | |
| ENST00000644184.2:c.3308T>C | ENSP00000495428.2:p.Leu1103Pro | |
| ENST00000645129.2:c.3194T>C | ENSP00000493639.2:p.Leu1065Pro | |
| ENST00000646440.2:c.3350T>C | ENSP00000495830.2:p.Leu1117Pro | |
| ENST00000298552.9:c.3350T>C MANE Select | ENSP00000298552.3:p.Leu1117Pro | |
| ENST00000642617.1:c.3347T>C | ENSP00000493773.1:p.Leu1116Pro | |
| ENST00000642627.1:c.3332T>C | ENSP00000496772.1:p.Leu1111Pro | |
| ENST00000642811.1:c.*3120T>C | ENSP00000495554.1:n.*3120T>C | |
| ENST00000643072.1:c.3197T>C | ENSP00000496691.1:p.Leu1066Pro | |
| ENST00000643583.1:c.3335T>C | ENSP00000494685.1:p.Leu1112Pro | |
| ENST00000643625.1:c.1227T>C | ENSP00000495546.1:n.1227T>C | |
| ENST00000643875.1:c.3350T>C | ENSP00000495158.1:p.Leu1117Pro | |
| ENST00000644097.1:c.3347T>C | ENSP00000494682.1:p.Leu1116Pro | |
| ENST00000644184.1:c.2045T>C | ENSP00000495428.1:p.Leu682Pro | |
| ENST00000644255.1:c.*3117T>C | ENSP00000493608.1:n.*3117T>C | |
| ENST00000644319.1:n.3725T>C | ||
| ENST00000644786.1:n.1009T>C | ||
| ENST00000644882.1:n.2258T>C | ||
| ENST00000645901.1:n.4201T>C | ||
| ENST00000646391.1:c.*3120T>C | ENSP00000494104.1:n.*3120T>C | |
| ENST00000646625.1:c.3350T>C | ENSP00000496263.1:p.Leu1117Pro | |
| ENST00000647262.1:n.2315T>C | ||
| ENST00000647279.1:c.*2589T>C | ENSP00000494502.1:n.*2589T>C | |
| ENST00000647534.1:n.2414T>C | ||
| ENST00000298552.7:c.3350T>C | ENSP00000298552.3:p.Leu1117Pro | |
| ENST00000440111.6:c.3350T>C | ENSP00000394524.2:p.Leu1117Pro | |
| ENST00000545250.5:c.3197T>C | ENSP00000444017.1:p.Leu1066Pro | |
| NM_000368.4:c.3350T>C , LRG_486t1:c.3350T>C | NP_000359.1:p.Leu1117Pro | |
| NM_001162426.1:c.3347T>C | NP_001155898.1:p.Leu1116Pro | |
| NM_001162427.1:c.3197T>C | NP_001155899.1:p.Leu1066Pro | |
| XM_005272211.1:c.3350T>C | XP_005272268.1:p.Leu1117Pro | |
| XM_006717271.1:c.3350T>C | XP_006717334.1:p.Leu1117Pro | |
| XM_011518979.1:c.3350T>C | XP_011517281.1:p.Leu1117Pro | |
| NM_001362177.1:c.2987T>C | NP_001349106.1:p.Leu996Pro | |
| XM_011518979.2:c.3350T>C | XP_011517281.1:p.Leu1117Pro | |
| XM_017015096.1:c.3350T>C | XP_016870585.1:p.Leu1117Pro | |
| XM_017015097.1:c.3350T>C | XP_016870586.1:p.Leu1117Pro | |
| XM_017015098.1:c.3347T>C | XP_016870587.1:p.Leu1116Pro | |
| XM_017015100.1:c.2987T>C | XP_016870589.1:p.Leu996Pro | |
| XM_017015101.1:c.2984T>C | XP_016870590.1:p.Leu995Pro | |
| NM_000368.5:c.3350T>C MANE Select | NP_000359.1:p.Leu1117Pro | |
| NM_001162426.2:c.3347T>C | NP_001155898.1:p.Leu1116Pro | |
| NM_001162427.2:c.3197T>C | NP_001155899.1:p.Leu1066Pro | |
| NM_001362177.2:c.2987T>C | NP_001349106.1:p.Leu996Pro |