Canonical Allele Identifier: CA1226125472
Gene: ACTA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.229431742T= , CM000663.2:g.229431742T= GRCh38
NC_000001.10:g.229567489T= , CM000663.1:g.229567489T= GRCh37
NC_000001.9:g.227634112T= NCBI36
NG_006672.1:g.7355A= , LRG_429:g.7355A=

Transcript Alleles

HGVS Amino-acid change
ENST00000366683.4:c.969A= ENSP00000355644.4:p.Ala323=
ENST00000684723.1:c.834A= ENSP00000508084.1:p.Ala278=
ENST00000366683.3:c.600A= ENSP00000355644.3:p.Ala200=
ENST00000366684.7:c.969A= MANE Select ENSP00000355645.3:p.Ala323=
NM_001100.3:c.969A= , LRG_429t1:c.969A= NP_001091.1:p.Ala323=
NM_001100.4:c.969A= MANE Select NP_001091.1:p.Ala323=