Canonical Allele Identifier: CA2123854602
Gene: TGM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.24259189C= , CM000676.2:g.24259189C= GRCh38
NC_000014.8:g.24728395C= , CM000676.1:g.24728395C= GRCh37
NC_000014.7:g.23798235C= NCBI36
NG_007150.1:g.8978G=
NG_007150.2:g.8978G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000206765.11:c.1045G= MANE Select ENSP00000206765.6:p.Gly349=
ENST00000206765.10:c.1045G= ENSP00000206765.6:p.Gly349=
ENST00000544573.5:c.-28-801G= ENSP00000439446.1:n.-28-801G=
ENST00000559136.1:c.118G= ENSP00000453337.1:p.Gly40=
NM_000359.2:c.1045G= NP_000350.1:p.Gly349=
NM_000359.3:c.1045G= MANE Select NP_000350.1:p.Gly349=