Canonical Allele Identifier: CA645556767

Gene: GCNT2

Linked Data

• COSMIC: COSM1329374

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.10529307_10529315del , CM000668.2:g.10529307_10529315del	GRCh38
NC_000006.11:g.10529540_10529548del , CM000668.1:g.10529540_10529548del	GRCh37
NC_000006.10:g.10637526_10637534del	NCBI36
NG_007469.3:g.42085_42093del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397423.7:n.484+466_484+474del
ENST00000495262.7:c.396_404del MANE Select	ENSP00000419411.2:p.Thr133_Ala135del
ENST00000379597.7:c.396_404del	ENSP00000368917.3:p.Thr133_Ala135del
ENST00000397423.6:n.484+466_484+474del
ENST00000410107.5:c.67+20149_67+20157del	ENSP00000386321.1:n.67+20149_67+20157del
ENST00000474518.1:n.508+466_508+474del
ENST00000474983.5:n.973_981del
ENST00000475577.5:n.254+1647_254+1655del
ENST00000483204.1:n.972_980del
ENST00000489225.5:n.283+36376_283+36384del
ENST00000489819.5:n.175+7713_175+7721del
ENST00000495262.5:c.396_404del	ENSP00000419411.1:p.Thr133_Ala135del
NM_145649.4:c.396_404del	NP_663624.1:p.Thr133_Ala135del
XM_005248999.2:c.165_173del	XP_005249056.1:p.Thr56_Ala58del
XM_006715052.2:c.396_404del	XP_006715115.1:p.Thr133_Ala135del
XM_006715053.2:c.396_404del	XP_006715116.1:p.Thr133_Ala135del
XM_011514465.1:c.396_404del	XP_011512767.1:p.Thr133_Ala135del
XM_011514467.1:c.165_173del	XP_011512769.1:p.Thr56_Ala58del
XM_011514468.1:c.396_404del	XP_011512770.1:p.Thr133_Ala135del
XR_926136.1:n.947_955del
XM_006715052.3:c.396_404del	XP_006715115.1:p.Thr133_Ala135del
XM_011514468.3:c.396_404del	XP_011512770.1:p.Thr133_Ala135del
XM_017010732.2:c.396_404del	XP_016866221.1:p.Thr133_Ala135del
XR_002956275.1:n.947_955del
XR_926136.2:n.945_953del
NM_001374747.1:c.396_404del	NP_001361676.1:p.Thr133_Ala135del
NM_145649.5:c.396_404del MANE Select	NP_663624.1:p.Thr133_Ala135del