Canonical Allele Identifier: CA345146317
Gene: ACTA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 617580
ClinVar RCV Id: RCV000754737
dbSNP Id: rs1301902450

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.229431904T>A , CM000663.2:g.229431904T>A GRCh38
NC_000001.10:g.229567651T>A , CM000663.1:g.229567651T>A GRCh37
NC_000001.9:g.227634274T>A NCBI36
NG_006672.1:g.7193A>T , LRG_429:g.7193A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000366683.4:c.809-2A>T ENSP00000355644.4:n.809-2A>T
ENST00000684723.1:c.674-2A>T ENSP00000508084.1:n.674-2A>T
ENST00000366683.3:c.480-42A>T ENSP00000355644.3:n.480-42A>T
ENST00000366684.7:c.809-2A>T MANE Select ENSP00000355645.3:n.809-2A>T
NM_001100.3:c.809-2A>T , LRG_429t1:c.809-2A>T NP_001091.1:n.809-2A>T
NM_001100.4:c.809-2A>T MANE Select NP_001091.1:n.809-2A>T