Canonical Allele Identifier: CA423754917
Gene: ACTA1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.229567648A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.229431901A>G , CM000663.2:g.229431901A>G GRCh38
NC_000001.10:g.229567648A>G , CM000663.1:g.229567648A>G GRCh37
NC_000001.9:g.227634271A>G NCBI36
NG_006672.1:g.7196T>C , LRG_429:g.7196T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000366683.4:c.810T>C ENSP00000355644.4:p.Gly270=
ENST00000684723.1:c.675T>C ENSP00000508084.1:p.Gly225=
ENST00000366683.3:c.480-39T>C ENSP00000355644.3:n.480-39T>C
ENST00000366684.7:c.810T>C MANE Select ENSP00000355645.3:p.Gly270=
NM_001100.3:c.810T>C , LRG_429t1:c.810T>C NP_001091.1:p.Gly270=
NM_001100.4:c.810T>C MANE Select NP_001091.1:p.Gly270=