Canonical Allele Identifier: CA2573051509
Gene: ACTA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1323848
ClinVar RCV Id: RCV001785881
dbSNP Id: rs2102735931

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.229432361_229432391del , CM000663.2:g.229432361_229432391del GRCh38
NC_000001.10:g.229568108_229568138del , CM000663.1:g.229568108_229568138del GRCh37
NC_000001.9:g.227634731_227634761del NCBI36
NG_006672.1:g.6709_6739del , LRG_429:g.6709_6739del

Transcript Alleles

HGVS Amino-acid change
ENST00000366683.4:c.498_528del ENSP00000355644.4:p.Ile167SerfsTer15
ENST00000684723.1:c.363_393del ENSP00000508084.1:p.Ile122SerfsTer15
ENST00000366683.3:c.479+19_479+49del ENSP00000355644.3:n.479+19_479+49del
ENST00000366684.7:c.498_528del MANE Select ENSP00000355645.3:p.Ile167SerfsTer15
NM_001100.3:c.498_528del , LRG_429t1:c.498_528del NP_001091.1:p.Ile167SerfsTer15
NM_001100.4:c.498_528del MANE Select NP_001091.1:p.Ile167SerfsTer15