Canonical Allele Identifier: CA1226125435
Gene: ACTA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.229431668A= , CM000663.2:g.229431668A= GRCh38
NC_000001.10:g.229567415A= , CM000663.1:g.229567415A= GRCh37
NC_000001.9:g.227634038A= NCBI36
NG_006672.1:g.7429T= , LRG_429:g.7429T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000366683.4:c.990+53T= ENSP00000355644.4:n.990+53T=
ENST00000684723.1:c.856-26T= ENSP00000508084.1:n.856-26T=
ENST00000366683.3:c.622-26T= ENSP00000355644.3:n.622-26T=
ENST00000366684.7:c.991-26T= MANE Select ENSP00000355645.3:n.991-26T=
NM_001100.3:c.991-26T= , LRG_429t1:c.991-26T= NP_001091.1:n.991-26T=
NM_001100.4:c.991-26T= MANE Select NP_001091.1:n.991-26T=