Canonical Allele Identifier: CA2173102675

Gene: TGM5

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43252905T= , CM000677.2:g.43252905T=	GRCh38
NC_000015.9:g.43545103T= , CM000677.1:g.43545103T=	GRCh37
NC_000015.8:g.41332395T=	NCBI36
NG_016124.1:g.18953A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220420.10:c.716A= MANE Select	ENSP00000220420.5:p.Asn239=
ENST00000635871.1:n.185A=
ENST00000220420.9:c.716A=	ENSP00000220420.5:p.Asn239=
ENST00000349114.8:c.470A=	ENSP00000220419.8:p.Asn157=
ENST00000610827.4:c.713A=	ENSP00000479732.1:p.Asn238=
ENST00000611276.4:c.467A=	ENSP00000482542.1:p.Asn156=
ENST00000622115.1:c.719A=	ENSP00000479638.1:p.Asn240=
NM_004245.3:c.470A=	NP_004236.1:p.Asn157=
NM_201631.3:c.716A=	NP_963925.2:p.Asn239=
XM_011522229.1:c.716A=	XP_011520531.1:p.Asn239=
XR_931948.1:n.890A=
NM_004245.4:c.470A=	NP_004236.1:p.Asn157=
NM_201631.4:c.716A= MANE Select	NP_963925.2:p.Asn239=