Canonical Allele Identifier: CA2123854528
Gene: TGM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.24259030_24259031delinsCT , CM000676.2:g.24259030_24259031delinsCT GRCh38
NC_000014.8:g.24728236_24728237delinsCT , CM000676.1:g.24728236_24728237delinsCT GRCh37
NC_000014.7:g.23798076_23798077delinsCT NCBI36
NG_007150.1:g.9136_9137delinsAG
NG_007150.2:g.9136_9137delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000206765.11:c.1159+44_1159+45delinsAG MANE Select ENSP00000206765.6:n.1159+44_1159+45delinsAG
ENST00000206765.10:c.1159+44_1159+45delinsAG ENSP00000206765.6:n.1159+44_1159+45delinsAG
ENST00000544573.5:c.-28-643_-28-642delinsAG ENSP00000439446.1:n.-28-643_-28-642delinsAG
ENST00000559136.1:c.232+44_232+45delinsAG ENSP00000453337.1:n.232+44_232+45delinsAG
NM_000359.2:c.1159+44_1159+45delinsAG NP_000350.1:n.1159+44_1159+45delinsAG
NM_000359.3:c.1159+44_1159+45delinsAG MANE Select NP_000350.1:n.1159+44_1159+45delinsAG