Canonical Allele Identifier: CA529915279
Gene: ACTA1 HGNC NCBI

Linked Data

dbSNP Id: rs1208506230

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.229432256G>A , CM000663.2:g.229432256G>A GRCh38
NC_000001.10:g.229568003G>A , CM000663.1:g.229568003G>A GRCh37
NC_000001.9:g.227634626G>A NCBI36
NG_006672.1:g.6841C>T , LRG_429:g.6841C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000366683.4:c.616+14C>T ENSP00000355644.4:n.616+14C>T
ENST00000684723.1:c.481+14C>T ENSP00000508084.1:n.481+14C>T
ENST00000366683.3:c.479+151C>T ENSP00000355644.3:n.479+151C>T
ENST00000366684.7:c.616+14C>T MANE Select ENSP00000355645.3:n.616+14C>T
NM_001100.3:c.616+14C>T , LRG_429t1:c.616+14C>T NP_001091.1:n.616+14C>T
NM_001100.4:c.616+14C>T MANE Select NP_001091.1:n.616+14C>T