Canonical Allele Identifier: CA2173102652

Gene: TGM5

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43252858A= , CM000677.2:g.43252858A=	GRCh38
NC_000015.9:g.43545056A= , CM000677.1:g.43545056A=	GRCh37
NC_000015.8:g.41332348A=	NCBI36
NG_016124.1:g.19000T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220420.10:c.763T= MANE Select	ENSP00000220420.5:p.Trp255=
ENST00000635871.1:n.232T=
ENST00000220420.9:c.763T=	ENSP00000220420.5:p.Trp255=
ENST00000349114.8:c.517T=	ENSP00000220419.8:p.Trp173=
ENST00000610827.4:c.760T=	ENSP00000479732.1:p.Trp254=
ENST00000611276.4:c.514T=	ENSP00000482542.1:p.Trp172=
ENST00000622115.1:c.766T=	ENSP00000479638.1:p.Trp256=
NM_004245.3:c.517T=	NP_004236.1:p.Trp173=
NM_201631.3:c.763T=	NP_963925.2:p.Trp255=
XM_011522229.1:c.763T=	XP_011520531.1:p.Trp255=
XR_931948.1:n.937T=
NM_004245.4:c.517T=	NP_004236.1:p.Trp173=
NM_201631.4:c.763T= MANE Select	NP_963925.2:p.Trp255=