Canonical Allele Identifier: CA1226125777
Gene: ACTA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.229432429T= , CM000663.2:g.229432429T= GRCh38
NC_000001.10:g.229568176T= , CM000663.1:g.229568176T= GRCh37
NC_000001.9:g.227634799T= NCBI36
NG_006672.1:g.6668A= , LRG_429:g.6668A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000366683.4:c.457A= ENSP00000355644.4:p.Ile153=
ENST00000684723.1:c.322A= ENSP00000508084.1:p.Ile108=
ENST00000366683.3:c.457A= ENSP00000355644.3:p.Ile153=
ENST00000366684.7:c.457A= MANE Select ENSP00000355645.3:p.Ile153=
NM_001100.3:c.457A= , LRG_429t1:c.457A= NP_001091.1:p.Ile153=
NM_001100.4:c.457A= MANE Select NP_001091.1:p.Ile153=