Canonical Allele Identifier: CA2173102601

Gene: TGM5

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43252765A= , CM000677.2:g.43252765A=	GRCh38
NC_000015.9:g.43544963A= , CM000677.1:g.43544963A=	GRCh37
NC_000015.8:g.41332255A=	NCBI36
NG_016124.1:g.19093T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000220420.10:c.856T= MANE Select	ENSP00000220420.5:p.Cys286=
ENST00000635871.1:n.325T=
ENST00000220420.9:c.856T=	ENSP00000220420.5:p.Cys286=
ENST00000349114.8:c.610T=	ENSP00000220419.8:p.Cys204=
ENST00000610827.4:c.853T=	ENSP00000479732.1:p.Cys285=
ENST00000611276.4:c.607T=	ENSP00000482542.1:p.Cys203=
ENST00000622115.1:c.859T=	ENSP00000479638.1:p.Cys287=
NM_004245.3:c.610T=	NP_004236.1:p.Cys204=
NM_201631.3:c.856T=	NP_963925.2:p.Cys286=
XM_011522229.1:c.856T=	XP_011520531.1:p.Cys286=
XR_931948.1:n.1030T=
NM_004245.4:c.610T=	NP_004236.1:p.Cys204=
NM_201631.4:c.856T= MANE Select	NP_963925.2:p.Cys286=