Canonical Allele Identifier: CA2525520724

Gene: GCNT2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.10529213_10529215dup , CM000668.2:g.10529213_10529215dup	GRCh38
NC_000006.11:g.10529446_10529448dup , CM000668.1:g.10529446_10529448dup	GRCh37
NC_000006.10:g.10637432_10637434dup	NCBI36
NG_007469.3:g.41991_41993dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397423.7:n.484+372_484+374dup
ENST00000483204.2:n.878_880dup
ENST00000495262.7:c.302_304dup MANE Select	ENSP00000419411.2:p.Val101_Thr102insMet
ENST00000379597.7:c.302_304dup	ENSP00000368917.3:p.Val101_Thr102insMet
ENST00000397423.6:n.484+372_484+374dup
ENST00000410107.5:c.67+20055_67+20057dup	ENSP00000386321.1:n.67+20055_67+20057dup
ENST00000474518.1:n.508+372_508+374dup
ENST00000474983.5:n.879_881dup
ENST00000475577.5:n.254+1553_254+1555dup
ENST00000483204.1:n.878_880dup
ENST00000489225.5:n.283+36282_283+36284dup
ENST00000489819.5:n.175+7619_175+7621dup
ENST00000495262.5:c.302_304dup	ENSP00000419411.1:p.Val101_Thr102insMet
NM_145649.4:c.302_304dup	NP_663624.1:p.Val101_Thr102insMet
XM_005248999.2:c.71_73dup	XP_005249056.1:p.Val24_Thr25insMet
XM_006715052.2:c.302_304dup	XP_006715115.1:p.Val101_Thr102insMet
XM_006715053.2:c.302_304dup	XP_006715116.1:p.Val101_Thr102insMet
XM_011514465.1:c.302_304dup	XP_011512767.1:p.Val101_Thr102insMet
XM_011514467.1:c.71_73dup	XP_011512769.1:p.Val24_Thr25insMet
XM_011514468.1:c.302_304dup	XP_011512770.1:p.Val101_Thr102insMet
XR_926136.1:n.853_855dup
XM_006715052.3:c.302_304dup	XP_006715115.1:p.Val101_Thr102insMet
XM_011514468.3:c.302_304dup	XP_011512770.1:p.Val101_Thr102insMet
XM_017010732.2:c.302_304dup	XP_016866221.1:p.Val101_Thr102insMet
XR_002956275.1:n.853_855dup
XR_926136.2:n.851_853dup
NM_001374747.1:c.302_304dup	NP_001361676.1:p.Val101_Thr102insMet
NM_145649.5:c.302_304dup MANE Select	NP_663624.1:p.Val101_Thr102insMet