Canonical Allele Identifier: CA2650926692
Gene: ACTA1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.229432456_229432459del , CM000663.2:g.229432456_229432459del GRCh38
NC_000001.10:g.229568203_229568206del , CM000663.1:g.229568203_229568206del GRCh37
NC_000001.9:g.227634826_227634829del NCBI36
NG_006672.1:g.6638_6641del , LRG_429:g.6638_6641del

Transcript Alleles

HGVS Amino-acid Change
ENST00000366683.4:c.455-28_455-25del ENSP00000355644.4:n.455-28_455-25del
ENST00000684723.1:c.320-28_320-25del ENSP00000508084.1:n.320-28_320-25del
ENST00000366683.3:c.455-28_455-25del ENSP00000355644.3:n.455-28_455-25del
ENST00000366684.7:c.455-28_455-25del MANE Select ENSP00000355645.3:n.455-28_455-25del
NM_001100.3:c.455-28_455-25del , LRG_429t1:c.455-28_455-25del NP_001091.1:n.455-28_455-25del
NM_001100.4:c.455-28_455-25del MANE Select NP_001091.1:n.455-28_455-25del