Canonical Allele Identifier: CA915942045
Gene: ACTA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 751078
ClinVar RCV Id: RCV000928102
dbSNP Id: rs1571892919

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.229431987G>C , CM000663.2:g.229431987G>C GRCh38
NC_000001.10:g.229567734G>C , CM000663.1:g.229567734G>C GRCh37
NC_000001.9:g.227634357G>C NCBI36
NG_006672.1:g.7110C>G , LRG_429:g.7110C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000366683.4:c.808+7C>G ENSP00000355644.4:n.808+7C>G
ENST00000684723.1:c.673+7C>G ENSP00000508084.1:n.673+7C>G
ENST00000366683.3:c.480-125C>G ENSP00000355644.3:n.480-125C>G
ENST00000366684.7:c.808+7C>G MANE Select ENSP00000355645.3:n.808+7C>G
NM_001100.3:c.808+7C>G , LRG_429t1:c.808+7C>G NP_001091.1:n.808+7C>G
NM_001100.4:c.808+7C>G MANE Select NP_001091.1:n.808+7C>G