Canonical Allele Identifier: CA2173103000

Gene: TGM5

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43253630T= , CM000677.2:g.43253630T=	GRCh38
NC_000015.9:g.43545828T= , CM000677.1:g.43545828T=	GRCh37
NC_000015.8:g.41333120T=	NCBI36
NG_016124.1:g.18228A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220420.10:c.560A= MANE Select	ENSP00000220420.5:p.Glu187=
ENST00000635871.1:n.29A=
ENST00000220420.9:c.560A=	ENSP00000220420.5:p.Glu187=
ENST00000349114.8:c.314A=	ENSP00000220419.8:p.Glu105=
ENST00000610827.4:c.557A=	ENSP00000479732.1:p.Glu186=
ENST00000611276.4:c.311A=	ENSP00000482542.1:p.Glu104=
ENST00000622115.1:c.563A=	ENSP00000479638.1:p.Glu188=
NM_004245.3:c.314A=	NP_004236.1:p.Glu105=
NM_201631.3:c.560A=	NP_963925.2:p.Glu187=
XM_011522229.1:c.560A=	XP_011520531.1:p.Glu187=
XR_931948.1:n.734A=
NM_004245.4:c.314A=	NP_004236.1:p.Glu105=
NM_201631.4:c.560A= MANE Select	NP_963925.2:p.Glu187=