Canonical Allele Identifier: CA916422665
Gene: ACTA1 HGNC NCBI

Linked Data

dbSNP Id: rs1558081539

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.229431929_229431930insTTCT , CM000663.2:g.229431929_229431930insTTCT GRCh38
NC_000001.10:g.229567676_229567677insTTCT , CM000663.1:g.229567676_229567677insTTCT GRCh37
NC_000001.9:g.227634299_227634300insTTCT NCBI36
NG_006672.1:g.7167_7168insAGAA , LRG_429:g.7167_7168insAGAA

Transcript Alleles

HGVS Amino-acid change
ENST00000366683.4:c.809-28_809-27insAGAA ENSP00000355644.4:n.809-28_809-27insAGAA
ENST00000684723.1:c.674-28_674-27insAGAA ENSP00000508084.1:n.674-28_674-27insAGAA
ENST00000366683.3:c.480-68_480-67insAGAA ENSP00000355644.3:n.480-68_480-67insAGAA
ENST00000366684.7:c.809-28_809-27insAGAA MANE Select ENSP00000355645.3:n.809-28_809-27insAGAA
NM_001100.3:c.809-28_809-27insAGAA , LRG_429t1:c.809-28_809-27insAGAA NP_001091.1:n.809-28_809-27insAGAA
NM_001100.4:c.809-28_809-27insAGAA MANE Select NP_001091.1:n.809-28_809-27insAGAA