Canonical Allele Identifier: CA1226125328
Gene: ACTA1 HGNC NCBI

Linked Data

dbSNP Id: rs1571892139
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.229431448A>C , CM000663.2:g.229431448A>C GRCh38
NC_000001.10:g.229567195A>C , CM000663.1:g.229567195A>C GRCh37
NC_000001.9:g.227633818A>C NCBI36
NG_006672.1:g.7649T>G , LRG_429:g.7649T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000366683.4:c.*51T>G ENSP00000355644.4:n.*51T>G
ENST00000684723.1:c.*51T>G ENSP00000508084.1:n.*51T>G
ENST00000366683.3:c.*51T>G ENSP00000355644.3:n.*51T>G
ENST00000366684.7:c.*51T>G MANE Select ENSP00000355645.3:n.*51T>G
NM_001100.3:c.*51T>G , LRG_429t1:c.*51T>G NP_001091.1:n.*51T>G
NM_001100.4:c.*51T>G MANE Select NP_001091.1:n.*51T>G
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Search 100 bp 3'