Canonical Allele Identifier: CA1226125702
Gene: ACTA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.229432241C= , CM000663.2:g.229432241C= GRCh38
NC_000001.10:g.229567988C= , CM000663.1:g.229567988C= GRCh37
NC_000001.9:g.227634611C= NCBI36
NG_006672.1:g.6856G= , LRG_429:g.6856G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000366683.4:c.616+29G= ENSP00000355644.4:n.616+29G=
ENST00000684723.1:c.481+29G= ENSP00000508084.1:n.481+29G=
ENST00000366683.3:c.479+166G= ENSP00000355644.3:n.479+166G=
ENST00000366684.7:c.616+29G= MANE Select ENSP00000355645.3:n.616+29G=
NM_001100.3:c.616+29G= , LRG_429t1:c.616+29G= NP_001091.1:n.616+29G=
NM_001100.4:c.616+29G= MANE Select NP_001091.1:n.616+29G=