Canonical Allele Identifier: CA2173103038

Gene: TGM5

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43253703C= , CM000677.2:g.43253703C=	GRCh38
NC_000015.9:g.43545901C= , CM000677.1:g.43545901C=	GRCh37
NC_000015.8:g.41333193C=	NCBI36
NG_016124.1:g.18155G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220420.10:c.556-69G= MANE Select	ENSP00000220420.5:n.556-69G=
ENST00000220420.9:c.556-69G=	ENSP00000220420.5:n.556-69G=
ENST00000349114.8:c.310-69G=	ENSP00000220419.8:n.310-69G=
ENST00000610827.4:c.553-69G=	ENSP00000479732.1:n.553-69G=
ENST00000611276.4:c.307-69G=	ENSP00000482542.1:n.307-69G=
ENST00000622115.1:c.559-69G=	ENSP00000479638.1:n.559-69G=
NM_004245.3:c.310-69G=	NP_004236.1:n.310-69G=
NM_201631.3:c.556-69G=	NP_963925.2:n.556-69G=
XM_011522229.1:c.556-69G=	XP_011520531.1:n.556-69G=
XR_931948.1:n.730-69G=
NM_004245.4:c.310-69G=	NP_004236.1:n.310-69G=
NM_201631.4:c.556-69G= MANE Select	NP_963925.2:n.556-69G=