Canonical Allele Identifier: CA423755292
Gene: ACTA1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.229568018T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.229432271T>A , CM000663.2:g.229432271T>A GRCh38
NC_000001.10:g.229568018T>A , CM000663.1:g.229568018T>A GRCh37
NC_000001.9:g.227634641T>A NCBI36
NG_006672.1:g.6826A>T , LRG_429:g.6826A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000366683.4:c.615A>T ENSP00000355644.4:p.Thr205=
ENST00000684723.1:c.480A>T ENSP00000508084.1:p.Thr160=
ENST00000366683.3:c.479+136A>T ENSP00000355644.3:n.479+136A>T
ENST00000366684.7:c.615A>T MANE Select ENSP00000355645.3:p.Thr205=
NM_001100.3:c.615A>T , LRG_429t1:c.615A>T NP_001091.1:p.Thr205=
NM_001100.4:c.615A>T MANE Select NP_001091.1:p.Thr205=