Canonical Allele Identifier: CA1226125500
Gene: ACTA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.229431823A= , CM000663.2:g.229431823A= GRCh38
NC_000001.10:g.229567570A= , CM000663.1:g.229567570A= GRCh37
NC_000001.9:g.227634193A= NCBI36
NG_006672.1:g.7274T= , LRG_429:g.7274T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000366683.4:c.888T= ENSP00000355644.4:p.Tyr296=
ENST00000684723.1:c.753T= ENSP00000508084.1:p.Tyr251=
ENST00000366683.3:c.519T= ENSP00000355644.3:p.Tyr173=
ENST00000366684.7:c.888T= MANE Select ENSP00000355645.3:p.Tyr296=
NM_001100.3:c.888T= , LRG_429t1:c.888T= NP_001091.1:p.Tyr296=
NM_001100.4:c.888T= MANE Select NP_001091.1:p.Tyr296=