Canonical Allele Identifier: CA2123856054
Gene: TGM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.24261988_24261989delinsAT , CM000676.2:g.24261988_24261989delinsAT GRCh38
NC_000014.8:g.24731194_24731195delinsAT , CM000676.1:g.24731194_24731195delinsAT GRCh37
NC_000014.7:g.23801034_23801035delinsAT NCBI36
NG_007150.1:g.6178_6179delinsAT
NG_007150.2:g.6178_6179delinsAT

Transcript Alleles

HGVS Amino-acid change
ENST00000206765.11:c.319+45_319+46delinsAT MANE Select ENSP00000206765.6:n.319+45_319+46delinsAT
ENST00000206765.10:c.319+45_319+46delinsAT ENSP00000206765.6:n.319+45_319+46delinsAT
ENST00000544573.5:c.-29+138_-29+139delinsAT ENSP00000439446.1:n.-29+138_-29+139delinsAT
ENST00000558074.1:c.319+45_319+46delinsAT ENSP00000453840.1:n.319+45_319+46delinsAT
NM_000359.2:c.319+45_319+46delinsAT NP_000350.1:n.319+45_319+46delinsAT
NM_000359.3:c.319+45_319+46delinsAT MANE Select NP_000350.1:n.319+45_319+46delinsAT