Canonical Allele Identifier: CA423755034
Gene: ACTA1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.229568105G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.229432358G>C , CM000663.2:g.229432358G>C GRCh38
NC_000001.10:g.229568105G>C , CM000663.1:g.229568105G>C GRCh37
NC_000001.9:g.227634728G>C NCBI36
NG_006672.1:g.6739C>G , LRG_429:g.6739C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000366683.4:c.528C>G ENSP00000355644.4:p.Ala176=
ENST00000684723.1:c.393C>G ENSP00000508084.1:p.Ala131=
ENST00000366683.3:c.479+49C>G ENSP00000355644.3:p.=
ENST00000366684.7:c.528C>G MANE Select ENSP00000355645.3:p.Ala176=
NM_001100.3:c.528C>G , LRG_429t1:c.528C>G NP_001091.1:p.Ala176=
NM_001100.4:c.528C>G MANE Select NP_001091.1:p.Ala176=