Canonical Allele Identifier: CA1610028592

Gene: GCNT2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.10529237_10529238delinsCT , CM000668.2:g.10529237_10529238delinsCT	GRCh38
NC_000006.11:g.10529470_10529471delinsCT , CM000668.1:g.10529470_10529471delinsCT	GRCh37
NC_000006.10:g.10637456_10637457delinsCT	NCBI36
NG_007469.3:g.42015_42016delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397423.7:n.484+396_484+397delinsCT
ENST00000483204.2:n.902_903delinsCT
ENST00000495262.7:c.326_327delinsCT MANE Select	ENSP00000419411.2:p.Thr109=
ENST00000379597.7:c.326_327delinsCT	ENSP00000368917.3:p.Thr109=
ENST00000397423.6:n.484+396_484+397delinsCT
ENST00000410107.5:c.67+20079_67+20080delinsCT	ENSP00000386321.1:n.67+20079_67+20080delinsCT
ENST00000474518.1:n.508+396_508+397delinsCT
ENST00000474983.5:n.903_904delinsCT
ENST00000475577.5:n.254+1577_254+1578delinsCT
ENST00000483204.1:n.902_903delinsCT
ENST00000489225.5:n.283+36306_283+36307delinsCT
ENST00000489819.5:n.175+7643_175+7644delinsCT
ENST00000495262.5:c.326_327delinsCT	ENSP00000419411.1:p.Thr109=
NM_145649.4:c.326_327delinsCT	NP_663624.1:p.Thr109=
XM_005248999.2:c.95_96delinsCT	XP_005249056.1:p.Thr32=
XM_006715052.2:c.326_327delinsCT	XP_006715115.1:p.Thr109=
XM_006715053.2:c.326_327delinsCT	XP_006715116.1:p.Thr109=
XM_011514465.1:c.326_327delinsCT	XP_011512767.1:p.Thr109=
XM_011514467.1:c.95_96delinsCT	XP_011512769.1:p.Thr32=
XM_011514468.1:c.326_327delinsCT	XP_011512770.1:p.Thr109=
XR_926136.1:n.877_878delinsCT
XM_006715052.3:c.326_327delinsCT	XP_006715115.1:p.Thr109=
XM_011514468.3:c.326_327delinsCT	XP_011512770.1:p.Thr109=
XM_017010732.2:c.326_327delinsCT	XP_016866221.1:p.Thr109=
XR_002956275.1:n.877_878delinsCT
XR_926136.2:n.875_876delinsCT
NM_001374747.1:c.326_327delinsCT	NP_001361676.1:p.Thr109=
NM_145649.5:c.326_327delinsCT MANE Select	NP_663624.1:p.Thr109=