Canonical Allele Identifier: CA1610029021

Gene: GCNT2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.10529439C= , CM000668.2:g.10529439C=	GRCh38
NC_000006.11:g.10529672C= , CM000668.1:g.10529672C=	GRCh37
NC_000006.10:g.10637658C=	NCBI36
NG_007469.3:g.42217C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397423.7:n.484+598C=
ENST00000495262.7:c.528C= MANE Select	ENSP00000419411.2:p.Asp176=
ENST00000379597.7:c.528C=	ENSP00000368917.3:p.Asp176=
ENST00000397423.6:n.484+598C=
ENST00000410107.5:c.67+20281C=	ENSP00000386321.1:n.67+20281C=
ENST00000474518.1:n.508+598C=
ENST00000474983.5:n.1105C=
ENST00000475577.5:n.254+1779C=
ENST00000483204.1:n.1104C=
ENST00000489225.5:n.283+36508C=
ENST00000489819.5:n.175+7845C=
ENST00000495262.5:c.528C=	ENSP00000419411.1:p.Asp176=
NM_145649.4:c.528C=	NP_663624.1:p.Asp176=
XM_005248999.2:c.297C=	XP_005249056.1:p.Asp99=
XM_006715052.2:c.528C=	XP_006715115.1:p.Asp176=
XM_006715053.2:c.528C=	XP_006715116.1:p.Asp176=
XM_011514465.1:c.528C=	XP_011512767.1:p.Asp176=
XM_011514467.1:c.297C=	XP_011512769.1:p.Asp99=
XM_011514468.1:c.528C=	XP_011512770.1:p.Asp176=
XR_926136.1:n.1079C=
XM_006715052.3:c.528C=	XP_006715115.1:p.Asp176=
XM_011514468.3:c.528C=	XP_011512770.1:p.Asp176=
XM_017010732.2:c.528C=	XP_016866221.1:p.Asp176=
XR_002956275.1:n.1079C=
XR_926136.2:n.1077C=
NM_001374747.1:c.528C=	NP_001361676.1:p.Asp176=
NM_145649.5:c.528C= MANE Select	NP_663624.1:p.Asp176=