Canonical Allele Identifier: CA2839675265
Gene: TGM5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.43253571dup , CM000677.2:g.43253571dup GRCh38
NC_000015.9:g.43545769dup , CM000677.1:g.43545769dup GRCh37
NC_000015.8:g.41333061dup NCBI36
NG_016124.1:g.18287dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000220420.10:c.619dup MANE Select ENSP00000220420.5:p.Asp207GlyfsTer27
ENST00000635871.1:n.88dup
ENST00000220420.9:c.619dup ENSP00000220420.5:p.Asp207GlyfsTer27
ENST00000349114.8:c.373dup ENSP00000220419.8:p.Asp125GlyfsTer27
ENST00000610827.4:c.616dup ENSP00000479732.1:p.Asp206GlyfsTer27
ENST00000611276.4:c.370dup ENSP00000482542.1:p.Asp124GlyfsTer27
ENST00000622115.1:c.622dup ENSP00000479638.1:p.Asp208GlyfsTer27
NM_004245.3:c.373dup NP_004236.1:p.Asp125GlyfsTer27
NM_201631.3:c.619dup NP_963925.2:p.Asp207GlyfsTer27
XM_011522229.1:c.619dup XP_011520531.1:p.Asp207GlyfsTer27
XR_931948.1:n.793dup
NM_004245.4:c.373dup NP_004236.1:p.Asp125GlyfsTer27
NM_201631.4:c.619dup MANE Select NP_963925.2:p.Asp207GlyfsTer27