Canonical Allele Identifier: CA2173102679

Gene: TGM5

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43252911A= , CM000677.2:g.43252911A=	GRCh38
NC_000015.9:g.43545109A= , CM000677.1:g.43545109A=	GRCh37
NC_000015.8:g.41332401A=	NCBI36
NG_016124.1:g.18947T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220420.10:c.710T= MANE Select	ENSP00000220420.5:p.Val237=
ENST00000635871.1:n.179T=
ENST00000220420.9:c.710T=	ENSP00000220420.5:p.Val237=
ENST00000349114.8:c.464T=	ENSP00000220419.8:p.Val155=
ENST00000610827.4:c.707T=	ENSP00000479732.1:p.Val236=
ENST00000611276.4:c.461T=	ENSP00000482542.1:p.Val154=
ENST00000622115.1:c.713T=	ENSP00000479638.1:p.Val238=
NM_004245.3:c.464T=	NP_004236.1:p.Val155=
NM_201631.3:c.710T=	NP_963925.2:p.Val237=
XM_011522229.1:c.710T=	XP_011520531.1:p.Val237=
XR_931948.1:n.884T=
NM_004245.4:c.464T=	NP_004236.1:p.Val155=
NM_201631.4:c.710T= MANE Select	NP_963925.2:p.Val237=