Canonical Allele Identifier: CA2173102645

Gene: TGM5

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43252847G= , CM000677.2:g.43252847G=	GRCh38
NC_000015.9:g.43545045G= , CM000677.1:g.43545045G=	GRCh37
NC_000015.8:g.41332337G=	NCBI36
NG_016124.1:g.19011C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220420.10:c.774C= MANE Select	ENSP00000220420.5:p.Ser258=
ENST00000635871.1:n.243C=
ENST00000220420.9:c.774C=	ENSP00000220420.5:p.Ser258=
ENST00000349114.8:c.528C=	ENSP00000220419.8:p.Ser176=
ENST00000610827.4:c.771C=	ENSP00000479732.1:p.Ser257=
ENST00000611276.4:c.525C=	ENSP00000482542.1:p.Ser175=
ENST00000622115.1:c.777C=	ENSP00000479638.1:p.Ser259=
NM_004245.3:c.528C=	NP_004236.1:p.Ser176=
NM_201631.3:c.774C=	NP_963925.2:p.Ser258=
XM_011522229.1:c.774C=	XP_011520531.1:p.Ser258=
XR_931948.1:n.948C=
NM_004245.4:c.528C=	NP_004236.1:p.Ser176=
NM_201631.4:c.774C= MANE Select	NP_963925.2:p.Ser258=