Canonical Allele Identifier: CA2173102580

Gene: TGM5

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43252734T= , CM000677.2:g.43252734T=	GRCh38
NC_000015.9:g.43544932T= , CM000677.1:g.43544932T=	GRCh37
NC_000015.8:g.41332224T=	NCBI36
NG_016124.1:g.19124A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220420.10:c.862+25A= MANE Select	ENSP00000220420.5:n.862+25A=
ENST00000635871.1:n.331+25A=
ENST00000220420.9:c.862+25A=	ENSP00000220420.5:n.862+25A=
ENST00000349114.8:c.616+25A=	ENSP00000220419.8:n.616+25A=
ENST00000610827.4:c.859+25A=	ENSP00000479732.1:n.859+25A=
ENST00000611276.4:c.613+25A=	ENSP00000482542.1:n.613+25A=
ENST00000622115.1:c.865+25A=	ENSP00000479638.1:n.865+25A=
NM_004245.3:c.616+25A=	NP_004236.1:n.616+25A=
NM_201631.3:c.862+25A=	NP_963925.2:n.862+25A=
XM_011522229.1:c.862+25A=	XP_011520531.1:n.862+25A=
XR_931948.1:n.1036+25A=
NM_004245.4:c.616+25A=	NP_004236.1:n.616+25A=
NM_201631.4:c.862+25A= MANE Select	NP_963925.2:n.862+25A=