Canonical Allele Identifier: CA2173102685

Gene: TGM5

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43252929C= , CM000677.2:g.43252929C=	GRCh38
NC_000015.9:g.43545127C= , CM000677.1:g.43545127C=	GRCh37
NC_000015.8:g.41332419C=	NCBI36
NG_016124.1:g.18929G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220420.10:c.692G= MANE Select	ENSP00000220420.5:p.Ser231=
ENST00000635871.1:n.161G=
ENST00000220420.9:c.692G=	ENSP00000220420.5:p.Ser231=
ENST00000349114.8:c.446G=	ENSP00000220419.8:p.Ser149=
ENST00000610827.4:c.689G=	ENSP00000479732.1:p.Ser230=
ENST00000611276.4:c.443G=	ENSP00000482542.1:p.Ser148=
ENST00000622115.1:c.695G=	ENSP00000479638.1:p.Ser232=
NM_004245.3:c.446G=	NP_004236.1:p.Ser149=
NM_201631.3:c.692G=	NP_963925.2:p.Ser231=
XM_011522229.1:c.692G=	XP_011520531.1:p.Ser231=
XR_931948.1:n.866G=
NM_004245.4:c.446G=	NP_004236.1:p.Ser149=
NM_201631.4:c.692G= MANE Select	NP_963925.2:p.Ser231=