Canonical Allele Identifier: CA2173102626

Gene: TGM5

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43252811G= , CM000677.2:g.43252811G=	GRCh38
NC_000015.9:g.43545009G= , CM000677.1:g.43545009G=	GRCh37
NC_000015.8:g.41332301G=	NCBI36
NG_016124.1:g.19047C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220420.10:c.810C= MANE Select	ENSP00000220420.5:p.Cys270=
ENST00000635871.1:n.279C=
ENST00000220420.9:c.810C=	ENSP00000220420.5:p.Cys270=
ENST00000349114.8:c.564C=	ENSP00000220419.8:p.Cys188=
ENST00000610827.4:c.807C=	ENSP00000479732.1:p.Cys269=
ENST00000611276.4:c.561C=	ENSP00000482542.1:p.Cys187=
ENST00000622115.1:c.813C=	ENSP00000479638.1:p.Cys271=
NM_004245.3:c.564C=	NP_004236.1:p.Cys188=
NM_201631.3:c.810C=	NP_963925.2:p.Cys270=
XM_011522229.1:c.810C=	XP_011520531.1:p.Cys270=
XR_931948.1:n.984C=
NM_004245.4:c.564C=	NP_004236.1:p.Cys188=
NM_201631.4:c.810C= MANE Select	NP_963925.2:p.Cys270=