Canonical Allele Identifier: CA1226125570
Gene: ACTA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.229431936_229431937delinsTC , CM000663.2:g.229431936_229431937delinsTC GRCh38
NC_000001.10:g.229567683_229567684delinsTC , CM000663.1:g.229567683_229567684delinsTC GRCh37
NC_000001.9:g.227634306_227634307delinsTC NCBI36
NG_006672.1:g.7160_7161delinsGA , LRG_429:g.7160_7161delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000366683.4:c.809-35_809-34delinsGA ENSP00000355644.4:n.809-35_809-34delinsGA
ENST00000684723.1:c.674-35_674-34delinsGA ENSP00000508084.1:n.674-35_674-34delinsGA
ENST00000366683.3:c.480-75_480-74delinsGA ENSP00000355644.3:n.480-75_480-74delinsGA
ENST00000366684.7:c.809-35_809-34delinsGA MANE Select ENSP00000355645.3:n.809-35_809-34delinsGA
NM_001100.3:c.809-35_809-34delinsGA , LRG_429t1:c.809-35_809-34delinsGA NP_001091.1:n.809-35_809-34delinsGA
NM_001100.4:c.809-35_809-34delinsGA MANE Select NP_001091.1:n.809-35_809-34delinsGA