Linked Data
ClinVar Variation Id:
217667
dbSNP Id:
rs540255320
ExAC:
14:58949430 G / A
gnomAD v2:
14-58949430-G-A
gnomAD v4:
14-58482712-G-A
PubMed:
PMID:26096313
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.58482712G>A , CM000676.2:g.58482712G>A | GRCh38 |
| NC_000014.8:g.58949430G>A , CM000676.1:g.58949430G>A | GRCh37 |
| NC_000014.7:g.58019183G>A | NCBI36 |
| NG_051335.2:g.60328G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000619722.5:c.2889G>A | ENSP00000481936.1:p.Pro963= | |
| ENST00000650845.1:n.3609G>A | ||
| ENST00000650904.1:c.3063G>A | ENSP00000498606.1:p.Pro1021= | |
| ENST00000651759.1:c.1812G>A | ENSP00000498415.1:p.Pro604= | |
| ENST00000651852.1:c.663G>A | ENSP00000498990.1:p.Pro221= | |
| ENST00000651937.1:c.*1347G>A | ENSP00000498785.1:n.*1347G>A | |
| ENST00000652326.2:c.3144G>A MANE Select | ENSP00000498929.1:p.Pro1048= | |
| ENST00000652414.1:c.1248G>A | ENSP00000498397.1:p.Pro416= | |
| ENST00000652732.1:c.*2629G>A | ENSP00000498799.1:n.*2629G>A | |
| ENST00000261244.9:c.2916G>A | ENSP00000261244.5:p.Pro972= | |
| ENST00000354386.10:c.3303G>A | ENSP00000346359.6:p.Pro1101= | |
| ENST00000423743.7:c.3012G>A | ENSP00000399427.3:p.Pro1004= | |
| ENST00000538571.6:n.2734G>A | ||
| ENST00000556134.5:c.3012G>A | ENSP00000452351.2:p.Pro1004= | |
| ENST00000619416.4:c.3099G>A | ENSP00000478083.1:p.Pro1033= | |
| ENST00000619722.4:c.2889G>A | ENSP00000481936.1:p.Pro963= | |
| NM_001244189.1:c.3303G>A | NP_001231118.1:p.Pro1101= | |
| NM_001244190.1:c.3099G>A | NP_001231119.1:p.Pro1033= | |
| NM_001244191.1:c.2889G>A | NP_001231120.1:p.Pro963= | |
| NM_001244192.1:c.3012G>A | NP_001231121.1:p.Pro1004= | |
| NM_001244193.1:c.2724G>A | NP_001231122.1:p.Pro908= | |
| NM_014749.3:c.2916G>A | NP_055564.3:p.Pro972= | |
| NM_001329943.2:c.3144G>A | NP_001316872.1:p.Pro1048= | |
| NM_001329944.1:c.3144G>A | NP_001316873.1:p.Pro1048= | |
| NM_001329945.1:c.2889G>A | NP_001316874.1:p.Pro963= | |
| NM_001329946.1:c.3144G>A | NP_001316875.1:p.Pro1048= | |
| NM_001329947.1:c.3144G>A | NP_001316876.1:p.Pro1048= | |
| NM_001364700.1:c.2889G>A | NP_001351629.1:p.Pro963= | |
| NM_001364701.1:c.2889G>A | NP_001351630.1:p.Pro963= | |
| NM_014749.4:c.2916G>A | NP_055564.3:p.Pro972= | |
| XM_024449779.1:c.3267G>A | XP_024305547.1:p.Pro1089= | |
| XM_024449780.1:c.3168G>A | XP_024305548.1:p.Pro1056= | |
| XM_024449781.1:c.3267G>A | XP_024305549.1:p.Pro1089= | |
| XM_024449782.1:c.2913G>A | XP_024305550.1:p.Pro971= | |
| XM_024449783.1:c.2913G>A | XP_024305551.1:p.Pro971= | |
| XM_024449784.1:c.2913G>A | XP_024305552.1:p.Pro971= | |
| XM_024449785.1:c.2889G>A | XP_024305553.1:p.Pro963= | |
| XM_024449787.1:c.2748G>A | XP_024305555.1:p.Pro916= | |
| XM_024449788.1:c.2724G>A | XP_024305556.1:p.Pro908= | |
| XM_024449789.1:c.2724G>A | XP_024305557.1:p.Pro908= | |
| XM_024449791.1:c.3168G>A | XP_024305559.1:p.Pro1056= | |
| NM_001244189.2:c.3303G>A | NP_001231118.1:p.Pro1101= | |
| NM_001244190.2:c.3099G>A | NP_001231119.1:p.Pro1033= | |
| NM_001244192.2:c.3012G>A | NP_001231121.1:p.Pro1004= | |
| NM_001329943.3:c.3144G>A MANE Select | NP_001316872.1:p.Pro1048= | |
| NM_001329944.2:c.3144G>A | NP_001316873.1:p.Pro1048= | |
| NM_001329945.2:c.2889G>A | NP_001316874.1:p.Pro963= | |
| NM_001329946.2:c.3144G>A | NP_001316875.1:p.Pro1048= | |
| NM_001329947.2:c.3144G>A | NP_001316876.1:p.Pro1048= | |
| NM_001364701.2:c.2889G>A | NP_001351630.1:p.Pro963= | |
| NM_014749.5:c.2916G>A | NP_055564.3:p.Pro972= | |
| NM_001244191.2:c.2889G>A | NP_001231120.1:p.Pro963= | |
| NM_001244193.2:c.2724G>A | NP_001231122.1:p.Pro908= |