Canonical Allele Identifier: CA916422666
Gene: ACTA1 HGNC NCBI

Linked Data

dbSNP Id: rs1558081542

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.229431932_229431934del , CM000663.2:g.229431932_229431934del GRCh38
NC_000001.10:g.229567679_229567681del , CM000663.1:g.229567679_229567681del GRCh37
NC_000001.9:g.227634302_227634304del NCBI36
NG_006672.1:g.7165_7167del , LRG_429:g.7165_7167del

Transcript Alleles

HGVS Amino-acid Change
ENST00000366683.4:c.809-30_809-28del ENSP00000355644.4:n.809-30_809-28del
ENST00000684723.1:c.674-30_674-28del ENSP00000508084.1:n.674-30_674-28del
ENST00000366683.3:c.480-70_480-68del ENSP00000355644.3:n.480-70_480-68del
ENST00000366684.7:c.809-30_809-28del MANE Select ENSP00000355645.3:n.809-30_809-28del
NM_001100.3:c.809-30_809-28del , LRG_429t1:c.809-30_809-28del NP_001091.1:n.809-30_809-28del
NM_001100.4:c.809-30_809-28del MANE Select NP_001091.1:n.809-30_809-28del