Canonical Allele Identifier: CA1226125569
Gene: ACTA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.229431935_229431936delinsCT , CM000663.2:g.229431935_229431936delinsCT GRCh38
NC_000001.10:g.229567682_229567683delinsCT , CM000663.1:g.229567682_229567683delinsCT GRCh37
NC_000001.9:g.227634305_227634306delinsCT NCBI36
NG_006672.1:g.7161_7162delinsAG , LRG_429:g.7161_7162delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000366683.4:c.809-34_809-33delinsAG ENSP00000355644.4:n.809-34_809-33delinsAG
ENST00000684723.1:c.674-34_674-33delinsAG ENSP00000508084.1:n.674-34_674-33delinsAG
ENST00000366683.3:c.480-74_480-73delinsAG ENSP00000355644.3:n.480-74_480-73delinsAG
ENST00000366684.7:c.809-34_809-33delinsAG MANE Select ENSP00000355645.3:n.809-34_809-33delinsAG
NM_001100.3:c.809-34_809-33delinsAG , LRG_429t1:c.809-34_809-33delinsAG NP_001091.1:n.809-34_809-33delinsAG
NM_001100.4:c.809-34_809-33delinsAG MANE Select NP_001091.1:n.809-34_809-33delinsAG