Canonical Allele Identifier: CA1226125228
Gene: ACTA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.229431326A= , CM000663.2:g.229431326A= GRCh38
NC_000001.10:g.229567073A= , CM000663.1:g.229567073A= GRCh37
NC_000001.9:g.227633696A= NCBI36
NG_006672.1:g.7771T= , LRG_429:g.7771T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000366683.4:c.*173T= ENSP00000355644.4:n.*173T=
ENST00000684723.1:c.*173T= ENSP00000508084.1:n.*173T=
ENST00000366683.3:c.*173T= ENSP00000355644.3:n.*173T=
ENST00000366684.7:c.*173T= MANE Select ENSP00000355645.3:n.*173T=
NM_001100.3:c.*173T= , LRG_429t1:c.*173T= NP_001091.1:n.*173T=
NM_001100.4:c.*173T= MANE Select NP_001091.1:n.*173T=