Canonical Allele Identifier: CA1226125329
Gene: ACTA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.229431449T= , CM000663.2:g.229431449T= GRCh38
NC_000001.10:g.229567196T= , CM000663.1:g.229567196T= GRCh37
NC_000001.9:g.227633819T= NCBI36
NG_006672.1:g.7648A= , LRG_429:g.7648A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000366683.4:c.*50A= ENSP00000355644.4:n.*50A=
ENST00000684723.1:c.*50A= ENSP00000508084.1:n.*50A=
ENST00000366683.3:c.*50A= ENSP00000355644.3:n.*50A=
ENST00000366684.7:c.*50A= MANE Select ENSP00000355645.3:n.*50A=
NM_001100.3:c.*50A= , LRG_429t1:c.*50A= NP_001091.1:n.*50A=
NM_001100.4:c.*50A= MANE Select NP_001091.1:n.*50A=