Canonical Allele Identifier: CA2173102606

Gene: TGM5

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43252770A= , CM000677.2:g.43252770A=	GRCh38
NC_000015.9:g.43544968A= , CM000677.1:g.43544968A=	GRCh37
NC_000015.8:g.41332260A=	NCBI36
NG_016124.1:g.19088T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000220420.10:c.851T= MANE Select	ENSP00000220420.5:p.Val284=
ENST00000635871.1:n.320T=
ENST00000220420.9:c.851T=	ENSP00000220420.5:p.Val284=
ENST00000349114.8:c.605T=	ENSP00000220419.8:p.Val202=
ENST00000610827.4:c.848T=	ENSP00000479732.1:p.Val283=
ENST00000611276.4:c.602T=	ENSP00000482542.1:p.Val201=
ENST00000622115.1:c.854T=	ENSP00000479638.1:p.Val285=
NM_004245.3:c.605T=	NP_004236.1:p.Val202=
NM_201631.3:c.851T=	NP_963925.2:p.Val284=
XM_011522229.1:c.851T=	XP_011520531.1:p.Val284=
XR_931948.1:n.1025T=
NM_004245.4:c.605T=	NP_004236.1:p.Val202=
NM_201631.4:c.851T= MANE Select	NP_963925.2:p.Val284=