Canonical Allele Identifier: CA1226125894
Gene: ACTA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.229432609A= , CM000663.2:g.229432609A= GRCh38
NC_000001.10:g.229568356A= , CM000663.1:g.229568356A= GRCh37
NC_000001.9:g.227634979A= NCBI36
NG_006672.1:g.6488T= , LRG_429:g.6488T=

Transcript Alleles

HGVS Amino-acid change
ENST00000366683.4:c.401T= ENSP00000355644.4:p.Met134=
ENST00000684723.1:c.266T= ENSP00000508084.1:p.Met89=
ENST00000366683.3:c.401T= ENSP00000355644.3:p.Met134=
ENST00000366684.7:c.401T= MANE Select ENSP00000355645.3:p.Met134=
NM_001100.3:c.401T= , LRG_429t1:c.401T= NP_001091.1:p.Met134=
NM_001100.4:c.401T= MANE Select NP_001091.1:p.Met134=