Canonical Allele Identifier: CA2173102964

Gene: TGM5

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43253550G= , CM000677.2:g.43253550G=	GRCh38
NC_000015.9:g.43545748G= , CM000677.1:g.43545748G=	GRCh37
NC_000015.8:g.41333040G=	NCBI36
NG_016124.1:g.18308C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220420.10:c.640C= MANE Select	ENSP00000220420.5:p.Leu214=
ENST00000635871.1:n.109C=
ENST00000220420.9:c.640C=	ENSP00000220420.5:p.Leu214=
ENST00000349114.8:c.394C=	ENSP00000220419.8:p.Leu132=
ENST00000610827.4:c.637C=	ENSP00000479732.1:p.Leu213=
ENST00000611276.4:c.391C=	ENSP00000482542.1:p.Leu131=
ENST00000622115.1:c.643C=	ENSP00000479638.1:p.Leu215=
NM_004245.3:c.394C=	NP_004236.1:p.Leu132=
NM_201631.3:c.640C=	NP_963925.2:p.Leu214=
XM_011522229.1:c.640C=	XP_011520531.1:p.Leu214=
XR_931948.1:n.814C=
NM_004245.4:c.394C=	NP_004236.1:p.Leu132=
NM_201631.4:c.640C= MANE Select	NP_963925.2:p.Leu214=