Canonical Allele Identifier: CA2173106049

Gene: TGM5

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43260468A= , CM000677.2:g.43260468A=	GRCh38
NC_000015.9:g.43552666A= , CM000677.1:g.43552666A=	GRCh37
NC_000015.8:g.41339958A=	NCBI36
NG_016124.1:g.11390T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220420.10:c.122T= MANE Select	ENSP00000220420.5:p.Leu41=
ENST00000220420.9:c.122T=	ENSP00000220420.5:p.Leu41=
ENST00000349114.8:c.122T=	ENSP00000220419.8:p.Leu41=
ENST00000610827.4:c.119T=	ENSP00000479732.1:p.Leu40=
ENST00000611276.4:c.119T=	ENSP00000482542.1:p.Leu40=
ENST00000622115.1:c.125T=	ENSP00000479638.1:p.Leu42=
NM_004245.3:c.122T=	NP_004236.1:p.Leu41=
NM_201631.3:c.122T=	NP_963925.2:p.Leu41=
XM_011522229.1:c.122T=	XP_011520531.1:p.Leu41=
XR_931948.1:n.296T=
NM_004245.4:c.122T=	NP_004236.1:p.Leu41=
NM_201631.4:c.122T= MANE Select	NP_963925.2:p.Leu41=