Canonical Allele Identifier: CA1610028491

Gene: GCNT2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.10529169_10529171delinsAAC , CM000668.2:g.10529169_10529171delinsAAC	GRCh38
NC_000006.11:g.10529402_10529404delinsAAC , CM000668.1:g.10529402_10529404delinsAAC	GRCh37
NC_000006.10:g.10637388_10637390delinsAAC	NCBI36
NG_007469.3:g.41947_41949delinsAAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397423.7:n.484+328_484+330delinsAAC
ENST00000483204.2:n.834_836delinsAAC
ENST00000495262.7:c.258_260delinsAAC MANE Select	ENSP00000419411.2:p.Glu86=
ENST00000379597.7:c.258_260delinsAAC	ENSP00000368917.3:p.Glu86=
ENST00000397423.6:n.484+328_484+330delinsAAC
ENST00000410107.5:c.67+20011_67+20013delinsAAC	ENSP00000386321.1:n.67+20011_67+20013delinsAAC
ENST00000474518.1:n.508+328_508+330delinsAAC
ENST00000474983.5:n.835_837delinsAAC
ENST00000475577.5:n.254+1509_254+1511delinsAAC
ENST00000483204.1:n.834_836delinsAAC
ENST00000489225.5:n.283+36238_283+36240delinsAAC
ENST00000489819.5:n.175+7575_175+7577delinsAAC
ENST00000495262.5:c.258_260delinsAAC	ENSP00000419411.1:p.Glu86=
NM_145649.4:c.258_260delinsAAC	NP_663624.1:p.Glu86=
XM_005248999.2:c.27_29delinsAAC	XP_005249056.1:p.Glu9=
XM_006715052.2:c.258_260delinsAAC	XP_006715115.1:p.Glu86=
XM_006715053.2:c.258_260delinsAAC	XP_006715116.1:p.Glu86=
XM_011514465.1:c.258_260delinsAAC	XP_011512767.1:p.Glu86=
XM_011514467.1:c.27_29delinsAAC	XP_011512769.1:p.Glu9=
XM_011514468.1:c.258_260delinsAAC	XP_011512770.1:p.Glu86=
XR_926136.1:n.809_811delinsAAC
XM_006715052.3:c.258_260delinsAAC	XP_006715115.1:p.Glu86=
XM_011514468.3:c.258_260delinsAAC	XP_011512770.1:p.Glu86=
XM_017010732.2:c.258_260delinsAAC	XP_016866221.1:p.Glu86=
XR_002956275.1:n.809_811delinsAAC
XR_926136.2:n.807_809delinsAAC
NM_001374747.1:c.258_260delinsAAC	NP_001361676.1:p.Glu86=
NM_145649.5:c.258_260delinsAAC MANE Select	NP_663624.1:p.Glu86=