Linked Data
ClinVar Variation Id:
199191
dbSNP Id:
rs142535134
ExAC:
4:5754591 C / T
gnomAD v2:
4-5754591-C-T
gnomAD v3:
4-5752864-C-T
gnomAD v4:
4-5752864-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.5752864C>T , CM000666.2:g.5752864C>T | GRCh38 |
| NC_000004.11:g.5754591C>T , CM000666.1:g.5754591C>T | GRCh37 |
| NC_000004.10:g.5805492C>T | NCBI36 |
| NG_008843.1:g.46668C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264956.11:c.1127C>T (EVC) MANE Select | ENSP00000264956.6:p.Ala376Val | |
| ENST00000264956.10:c.1127C>T (EVC) | ENSP00000264956.6:p.Ala376Val | |
| ENST00000506216.5:n.1648-4552G>A (CRMP1) | ||
| ENST00000509451.1:c.1127C>T (EVC) | ENSP00000426774.1:p.Ala376Val | |
| ENST00000514919.1:n.190C>T (EVC) | ||
| NM_001306090.1:c.1127C>T (EVC) | NP_001293019.1:p.Ala376Val | |
| NM_001306092.1:c.1127C>T (EVC) | NP_001293021.1:p.Ala376Val | |
| NM_153717.2:c.1127C>T (EVC) | NP_714928.1:p.Ala376Val | |
| XM_006713865.2:c.1127C>T (EVC) | XP_006713928.1:p.Ala376Val | |
| XM_006713866.2:c.1127C>T (EVC) | XP_006713929.1:p.Ala376Val | |
| XM_011513419.1:c.1127C>T (EVC) | XP_011511721.1:p.Ala376Val | |
| XR_427473.2:n.1317C>T (EVC) | ||
| XR_427475.2:n.1317C>T (EVC) | ||
| XR_427476.2:n.1317C>T (EVC) | ||
| XR_924920.1:n.1317C>T (EVC) | ||
| XR_924921.1:n.1317C>T (EVC) | ||
| XR_924922.1:n.1317C>T (EVC) | ||
| XR_924923.1:n.1317C>T (EVC) | ||
| XR_924924.1:n.1317C>T (EVC) | ||
| XR_924925.1:n.1317C>T (EVC) | ||
| XR_924926.1:n.1317C>T (EVC) | ||
| XR_924927.1:n.1317C>T (EVC) | ||
| XR_924928.1:n.1319C>T (EVC) | ||
| XM_006713865.3:c.1127C>T (EVC) | XP_006713928.1:p.Ala376Val | |
| XM_006713866.3:c.1127C>T (EVC) | XP_006713929.1:p.Ala376Val | |
| XM_011513419.2:c.1127C>T (EVC) | XP_011511721.1:p.Ala376Val | |
| XM_017007883.2:c.1127C>T (EVC) | XP_016863372.1:p.Ala376Val | |
| XR_001741164.1:n.1307C>T (EVC) | ||
| XR_001741165.1:n.1307C>T (EVC) | ||
| XR_001741166.1:n.1307C>T (EVC) | ||
| XR_001741167.1:n.1307C>T (EVC) | ||
| XR_001741168.1:n.1307C>T (EVC) | ||
| XR_001741169.2:n.1171C>T (EVC) | ||
| XR_001741170.1:n.1309C>T (EVC) | ||
| XR_001741171.1:n.612C>T (EVC) | ||
| XR_427473.3:n.1307C>T (EVC) | ||
| XR_427475.3:n.1307C>T (EVC) | ||
| XR_427476.3:n.1307C>T (EVC) | ||
| XR_924920.2:n.1307C>T (EVC) | ||
| XR_924921.2:n.1307C>T (EVC) | ||
| XR_924922.2:n.1307C>T (EVC) | ||
| XR_924924.2:n.1307C>T (EVC) | ||
| XR_924925.2:n.1307C>T (EVC) | ||
| XR_924926.2:n.1307C>T (EVC) | ||
| NM_153717.3:c.1127C>T (EVC) MANE Select | NP_714928.1:p.Ala376Val | |
| NM_001306090.2:c.1127C>T (EVC) | NP_001293019.1:p.Ala376Val | |
| NM_001306092.2:c.1127C>T (EVC) | NP_001293021.1:p.Ala376Val |