Linked Data
dbSNP Id:
rs374813665
ExAC:
4:5754761 G / T
gnomAD v2:
4-5754761-G-T
gnomAD v3:
4-5753034-G-T
gnomAD v4:
4-5753034-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.5753034G>T , CM000666.2:g.5753034G>T | GRCh38 |
| NC_000004.11:g.5754761G>T , CM000666.1:g.5754761G>T | GRCh37 |
| NC_000004.10:g.5805662G>T | NCBI36 |
| NG_008843.1:g.46838G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264956.11:c.1297G>T (EVC) MANE Select | ENSP00000264956.6:p.Ala433Ser | |
| ENST00000264956.10:c.1297G>T (EVC) | ENSP00000264956.6:p.Ala433Ser | |
| ENST00000506216.5:n.1648-4722C>A (CRMP1) | ||
| ENST00000509451.1:c.1297G>T (EVC) | ENSP00000426774.1:p.Ala433Ser | |
| ENST00000514919.1:n.360G>T (EVC) | ||
| NM_001306090.1:c.1297G>T (EVC) | NP_001293019.1:p.Ala433Ser | |
| NM_001306092.1:c.1297G>T (EVC) | NP_001293021.1:p.Ala433Ser | |
| NM_153717.2:c.1297G>T (EVC) | NP_714928.1:p.Ala433Ser | |
| XM_006713865.2:c.1297G>T (EVC) | XP_006713928.1:p.Ala433Ser | |
| XM_006713866.2:c.1297G>T (EVC) | XP_006713929.1:p.Ala433Ser | |
| XM_011513419.1:c.1297G>T (EVC) | XP_011511721.1:p.Ala433Ser | |
| XR_427473.2:n.1487G>T (EVC) | ||
| XR_427475.2:n.1487G>T (EVC) | ||
| XR_427476.2:n.1487G>T (EVC) | ||
| XR_924920.1:n.1487G>T (EVC) | ||
| XR_924921.1:n.1487G>T (EVC) | ||
| XR_924922.1:n.1487G>T (EVC) | ||
| XR_924923.1:n.1487G>T (EVC) | ||
| XR_924924.1:n.1487G>T (EVC) | ||
| XR_924925.1:n.1487G>T (EVC) | ||
| XR_924926.1:n.1487G>T (EVC) | ||
| XR_924927.1:n.1487G>T (EVC) | ||
| XR_924928.1:n.1489G>T (EVC) | ||
| XM_006713865.3:c.1297G>T (EVC) | XP_006713928.1:p.Ala433Ser | |
| XM_006713866.3:c.1297G>T (EVC) | XP_006713929.1:p.Ala433Ser | |
| XM_011513419.2:c.1297G>T (EVC) | XP_011511721.1:p.Ala433Ser | |
| XM_017007883.2:c.1297G>T (EVC) | XP_016863372.1:p.Ala433Ser | |
| XR_001741164.1:n.1477G>T (EVC) | ||
| XR_001741165.1:n.1477G>T (EVC) | ||
| XR_001741166.1:n.1477G>T (EVC) | ||
| XR_001741167.1:n.1477G>T (EVC) | ||
| XR_001741168.1:n.1477G>T (EVC) | ||
| XR_001741169.2:n.1341G>T (EVC) | ||
| XR_001741170.1:n.1479G>T (EVC) | ||
| XR_001741171.1:n.782G>T (EVC) | ||
| XR_427473.3:n.1477G>T (EVC) | ||
| XR_427475.3:n.1477G>T (EVC) | ||
| XR_427476.3:n.1477G>T (EVC) | ||
| XR_924920.2:n.1477G>T (EVC) | ||
| XR_924921.2:n.1477G>T (EVC) | ||
| XR_924922.2:n.1477G>T (EVC) | ||
| XR_924924.2:n.1477G>T (EVC) | ||
| XR_924925.2:n.1477G>T (EVC) | ||
| XR_924926.2:n.1477G>T (EVC) | ||
| NM_153717.3:c.1297G>T (EVC) MANE Select | NP_714928.1:p.Ala433Ser | |
| NM_001306090.2:c.1297G>T (EVC) | NP_001293019.1:p.Ala433Ser | |
| NM_001306092.2:c.1297G>T (EVC) | NP_001293021.1:p.Ala433Ser |