Canonical Allele Identifier: CA2173102967

Gene: TGM5

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43253556A= , CM000677.2:g.43253556A=	GRCh38
NC_000015.9:g.43545754A= , CM000677.1:g.43545754A=	GRCh37
NC_000015.8:g.41333046A=	NCBI36
NG_016124.1:g.18302T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000220420.10:c.634T= MANE Select	ENSP00000220420.5:p.Cys212=
ENST00000635871.1:n.103T=
ENST00000220420.9:c.634T=	ENSP00000220420.5:p.Cys212=
ENST00000349114.8:c.388T=	ENSP00000220419.8:p.Cys130=
ENST00000610827.4:c.631T=	ENSP00000479732.1:p.Cys211=
ENST00000611276.4:c.385T=	ENSP00000482542.1:p.Cys129=
ENST00000622115.1:c.637T=	ENSP00000479638.1:p.Cys213=
NM_004245.3:c.388T=	NP_004236.1:p.Cys130=
NM_201631.3:c.634T=	NP_963925.2:p.Cys212=
XM_011522229.1:c.634T=	XP_011520531.1:p.Cys212=
XR_931948.1:n.808T=
NM_004245.4:c.388T=	NP_004236.1:p.Cys130=
NM_201631.4:c.634T= MANE Select	NP_963925.2:p.Cys212=