Canonical Allele Identifier: CA2173102622

Gene: TGM5

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43252803A= , CM000677.2:g.43252803A=	GRCh38
NC_000015.9:g.43545001A= , CM000677.1:g.43545001A=	GRCh37
NC_000015.8:g.41332293A=	NCBI36
NG_016124.1:g.19055T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220420.10:c.818T= MANE Select	ENSP00000220420.5:p.Val273=
ENST00000635871.1:n.287T=
ENST00000220420.9:c.818T=	ENSP00000220420.5:p.Val273=
ENST00000349114.8:c.572T=	ENSP00000220419.8:p.Val191=
ENST00000610827.4:c.815T=	ENSP00000479732.1:p.Val272=
ENST00000611276.4:c.569T=	ENSP00000482542.1:p.Val190=
ENST00000622115.1:c.821T=	ENSP00000479638.1:p.Val274=
NM_004245.3:c.572T=	NP_004236.1:p.Val191=
NM_201631.3:c.818T=	NP_963925.2:p.Val273=
XM_011522229.1:c.818T=	XP_011520531.1:p.Val273=
XR_931948.1:n.992T=
NM_004245.4:c.572T=	NP_004236.1:p.Val191=
NM_201631.4:c.818T= MANE Select	NP_963925.2:p.Val273=