Canonical Allele Identifier: CA1226125325
Gene: ACTA1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.229431447C= , CM000663.2:g.229431447C= GRCh38
NC_000001.10:g.229567194C= , CM000663.1:g.229567194C= GRCh37
NC_000001.9:g.227633817C= NCBI36
NG_006672.1:g.7650G= , LRG_429:g.7650G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000366683.4:c.*52G= ENSP00000355644.4:n.*52G=
ENST00000684723.1:c.*52G= ENSP00000508084.1:n.*52G=
ENST00000366683.3:c.*52G= ENSP00000355644.3:n.*52G=
ENST00000366684.7:c.*52G= MANE Select ENSP00000355645.3:n.*52G=
NM_001100.3:c.*52G= , LRG_429t1:c.*52G= NP_001091.1:n.*52G=
NM_001100.4:c.*52G= MANE Select NP_001091.1:n.*52G=
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