Canonical Allele Identifier: CA2173102598

Gene: TGM5

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43252759C= , CM000677.2:g.43252759C=	GRCh38
NC_000015.9:g.43544957C= , CM000677.1:g.43544957C=	GRCh37
NC_000015.8:g.41332249C=	NCBI36
NG_016124.1:g.19099G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000220420.10:c.862G= MANE Select	ENSP00000220420.5:p.Val288=
ENST00000635871.1:n.331G=
ENST00000220420.9:c.862G=	ENSP00000220420.5:p.Val288=
ENST00000349114.8:c.616G=	ENSP00000220419.8:p.Val206=
ENST00000610827.4:c.859G=	ENSP00000479732.1:p.Val287=
ENST00000611276.4:c.613G=	ENSP00000482542.1:p.Val205=
ENST00000622115.1:c.865G=	ENSP00000479638.1:p.Val289=
NM_004245.3:c.616G=	NP_004236.1:p.Val206=
NM_201631.3:c.862G=	NP_963925.2:p.Val288=
XM_011522229.1:c.862G=	XP_011520531.1:p.Val288=
XR_931948.1:n.1036G=
NM_004245.4:c.616G=	NP_004236.1:p.Val206=
NM_201631.4:c.862G= MANE Select	NP_963925.2:p.Val288=