Canonical Allele Identifier: CA1226125281
Gene: ACTA1 HGNC NCBI

Linked Data

dbSNP Id: rs1659929374

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.229431407A>G , CM000663.2:g.229431407A>G GRCh38
NC_000001.10:g.229567154A>G , CM000663.1:g.229567154A>G GRCh37
NC_000001.9:g.227633777A>G NCBI36
NG_006672.1:g.7690T>C , LRG_429:g.7690T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000366683.4:c.*92T>C ENSP00000355644.4:n.*92T>C
ENST00000684723.1:c.*92T>C ENSP00000508084.1:n.*92T>C
ENST00000366683.3:c.*92T>C ENSP00000355644.3:n.*92T>C
ENST00000366684.7:c.*92T>C MANE Select ENSP00000355645.3:n.*92T>C
NM_001100.3:c.*92T>C , LRG_429t1:c.*92T>C NP_001091.1:n.*92T>C
NM_001100.4:c.*92T>C MANE Select NP_001091.1:n.*92T>C