Canonical Allele Identifier: CA2173102648

Gene: TGM5

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43252853C= , CM000677.2:g.43252853C=	GRCh38
NC_000015.9:g.43545051C= , CM000677.1:g.43545051C=	GRCh37
NC_000015.8:g.41332343C=	NCBI36
NG_016124.1:g.19005G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220420.10:c.768G= MANE Select	ENSP00000220420.5:p.Thr256=
ENST00000635871.1:n.237G=
ENST00000220420.9:c.768G=	ENSP00000220420.5:p.Thr256=
ENST00000349114.8:c.522G=	ENSP00000220419.8:p.Thr174=
ENST00000610827.4:c.765G=	ENSP00000479732.1:p.Thr255=
ENST00000611276.4:c.519G=	ENSP00000482542.1:p.Thr173=
ENST00000622115.1:c.771G=	ENSP00000479638.1:p.Thr257=
NM_004245.3:c.522G=	NP_004236.1:p.Thr174=
NM_201631.3:c.768G=	NP_963925.2:p.Thr256=
XM_011522229.1:c.768G=	XP_011520531.1:p.Thr256=
XR_931948.1:n.942G=
NM_004245.4:c.522G=	NP_004236.1:p.Thr174=
NM_201631.4:c.768G= MANE Select	NP_963925.2:p.Thr256=