Canonical Allele Identifier: CA2173102698

Gene: TGM5

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43252956A= , CM000677.2:g.43252956A=	GRCh38
NC_000015.9:g.43545154A= , CM000677.1:g.43545154A=	GRCh37
NC_000015.8:g.41332446A=	NCBI36
NG_016124.1:g.18902T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220420.10:c.685-20T= MANE Select	ENSP00000220420.5:n.685-20T=
ENST00000635871.1:n.154-20T=
ENST00000220420.9:c.685-20T=	ENSP00000220420.5:n.685-20T=
ENST00000349114.8:c.439-20T=	ENSP00000220419.8:n.439-20T=
ENST00000610827.4:c.682-20T=	ENSP00000479732.1:n.682-20T=
ENST00000611276.4:c.436-20T=	ENSP00000482542.1:n.436-20T=
ENST00000622115.1:c.688-20T=	ENSP00000479638.1:n.688-20T=
NM_004245.3:c.439-20T=	NP_004236.1:n.439-20T=
NM_201631.3:c.685-20T=	NP_963925.2:n.685-20T=
XM_011522229.1:c.685-20T=	XP_011520531.1:n.685-20T=
XR_931948.1:n.859-20T=
NM_004245.4:c.439-20T=	NP_004236.1:n.439-20T=
NM_201631.4:c.685-20T= MANE Select	NP_963925.2:n.685-20T=