Canonical Allele Identifier: CA1610028622

Gene: GCNT2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.10529259_10529275delinsGATTTATATGCCCCAAA , CM000668.2:g.10529259_10529275delinsGATTTATATGCCCCAAA	GRCh38
NC_000006.11:g.10529492_10529508delinsGATTTATATGCCCCAAA , CM000668.1:g.10529492_10529508delinsGATTTATATGCCCCAAA	GRCh37
NC_000006.10:g.10637478_10637494delinsGATTTATATGCCCCAAA	NCBI36
NG_007469.3:g.42037_42053delinsGATTTATATGCCCCAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397423.7:n.484+418_484+434delinsGATTTATATGCCCCAAA
ENST00000483204.2:n.924_940delinsGATTTATATGCCCCAAA
ENST00000495262.7:c.348_364delinsGATTTATATGCCCCAAA MANE Select	ENSP00000419411.2:p.Ala116=
ENST00000379597.7:c.348_364delinsGATTTATATGCCCCAAA	ENSP00000368917.3:p.Ala116=
ENST00000397423.6:n.484+418_484+434delinsGATTTATATGCCCCAAA
ENST00000410107.5:c.67+20101_67+20117delinsGATTTATATGCCCCAAA	ENSP00000386321.1:n.67+20101_67+20117delinsGATTTATATGCCCCAAA
ENST00000474518.1:n.508+418_508+434delinsGATTTATATGCCCCAAA
ENST00000474983.5:n.925_941delinsGATTTATATGCCCCAAA
ENST00000475577.5:n.254+1599_254+1615delinsGATTTATATGCCCCAAA
ENST00000483204.1:n.924_940delinsGATTTATATGCCCCAAA
ENST00000489225.5:n.283+36328_283+36344delinsGATTTATATGCCCCAAA
ENST00000489819.5:n.175+7665_175+7681delinsGATTTATATGCCCCAAA
ENST00000495262.5:c.348_364delinsGATTTATATGCCCCAAA	ENSP00000419411.1:p.Ala116=
NM_145649.4:c.348_364delinsGATTTATATGCCCCAAA	NP_663624.1:p.Ala116=
XM_005248999.2:c.117_133delinsGATTTATATGCCCCAAA	XP_005249056.1:p.Ala39=
XM_006715052.2:c.348_364delinsGATTTATATGCCCCAAA	XP_006715115.1:p.Ala116=
XM_006715053.2:c.348_364delinsGATTTATATGCCCCAAA	XP_006715116.1:p.Ala116=
XM_011514465.1:c.348_364delinsGATTTATATGCCCCAAA	XP_011512767.1:p.Ala116=
XM_011514467.1:c.117_133delinsGATTTATATGCCCCAAA	XP_011512769.1:p.Ala39=
XM_011514468.1:c.348_364delinsGATTTATATGCCCCAAA	XP_011512770.1:p.Ala116=
XR_926136.1:n.899_915delinsGATTTATATGCCCCAAA
XM_006715052.3:c.348_364delinsGATTTATATGCCCCAAA	XP_006715115.1:p.Ala116=
XM_011514468.3:c.348_364delinsGATTTATATGCCCCAAA	XP_011512770.1:p.Ala116=
XM_017010732.2:c.348_364delinsGATTTATATGCCCCAAA	XP_016866221.1:p.Ala116=
XR_002956275.1:n.899_915delinsGATTTATATGCCCCAAA
XR_926136.2:n.897_913delinsGATTTATATGCCCCAAA
NM_001374747.1:c.348_364delinsGATTTATATGCCCCAAA	NP_001361676.1:p.Ala116=
NM_145649.5:c.348_364delinsGATTTATATGCCCCAAA MANE Select	NP_663624.1:p.Ala116=