Canonical Allele Identifier: CA2123854742
Gene: TGM1 HGNC NCBI

Linked Data

dbSNP Id: rs2040786533

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.24259462del , CM000676.2:g.24259462del GRCh38
NC_000014.8:g.24728668del , CM000676.1:g.24728668del GRCh37
NC_000014.7:g.23798508del NCBI36
NG_007150.1:g.8707del
NG_007150.2:g.8707del

Transcript Alleles

HGVS Amino-acid Change
ENST00000206765.11:c.985-211del MANE Select ENSP00000206765.6:n.985-211del
ENST00000206765.10:c.985-211del ENSP00000206765.6:n.985-211del
ENST00000544573.5:c.-28-1072del ENSP00000439446.1:n.-28-1072del
ENST00000559136.1:c.58-211del ENSP00000453337.1:n.58-211del
NM_000359.2:c.985-211del NP_000350.1:n.985-211del
NM_000359.3:c.985-211del MANE Select NP_000350.1:n.985-211del