Canonical Allele Identifier: CA1226125645
Gene: ACTA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.229432094G= , CM000663.2:g.229432094G= GRCh38
NC_000001.10:g.229567841G= , CM000663.1:g.229567841G= GRCh37
NC_000001.9:g.227634464G= NCBI36
NG_006672.1:g.7003C= , LRG_429:g.7003C=

Transcript Alleles

HGVS Amino-acid change
ENST00000366683.4:c.708C= ENSP00000355644.4:p.Ser236=
ENST00000684723.1:c.573C= ENSP00000508084.1:p.Ser191=
ENST00000366683.3:c.480-232C= ENSP00000355644.3:n.480-232C=
ENST00000366684.7:c.708C= MANE Select ENSP00000355645.3:p.Ser236=
NM_001100.3:c.708C= , LRG_429t1:c.708C= NP_001091.1:p.Ser236=
NM_001100.4:c.708C= MANE Select NP_001091.1:p.Ser236=