Canonical Allele Identifier: CA1610028487

Gene: GCNT2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.10529165_10529167delinsCAG , CM000668.2:g.10529165_10529167delinsCAG	GRCh38
NC_000006.11:g.10529398_10529400delinsCAG , CM000668.1:g.10529398_10529400delinsCAG	GRCh37
NC_000006.10:g.10637384_10637386delinsCAG	NCBI36
NG_007469.3:g.41943_41945delinsCAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397423.7:n.484+324_484+326delinsCAG
ENST00000483204.2:n.830_832delinsCAG
ENST00000495262.7:c.254_256delinsCAG MANE Select	ENSP00000419411.2:p.Thr85=
ENST00000379597.7:c.254_256delinsCAG	ENSP00000368917.3:p.Thr85=
ENST00000397423.6:n.484+324_484+326delinsCAG
ENST00000410107.5:c.67+20007_67+20009delinsCAG	ENSP00000386321.1:n.67+20007_67+20009delinsCAG
ENST00000474518.1:n.508+324_508+326delinsCAG
ENST00000474983.5:n.831_833delinsCAG
ENST00000475577.5:n.254+1505_254+1507delinsCAG
ENST00000483204.1:n.830_832delinsCAG
ENST00000489225.5:n.283+36234_283+36236delinsCAG
ENST00000489819.5:n.175+7571_175+7573delinsCAG
ENST00000495262.5:c.254_256delinsCAG	ENSP00000419411.1:p.Thr85=
NM_145649.4:c.254_256delinsCAG	NP_663624.1:p.Thr85=
XM_005248999.2:c.23_25delinsCAG	XP_005249056.1:p.Thr8=
XM_006715052.2:c.254_256delinsCAG	XP_006715115.1:p.Thr85=
XM_006715053.2:c.254_256delinsCAG	XP_006715116.1:p.Thr85=
XM_011514465.1:c.254_256delinsCAG	XP_011512767.1:p.Thr85=
XM_011514467.1:c.23_25delinsCAG	XP_011512769.1:p.Thr8=
XM_011514468.1:c.254_256delinsCAG	XP_011512770.1:p.Thr85=
XR_926136.1:n.805_807delinsCAG
XM_006715052.3:c.254_256delinsCAG	XP_006715115.1:p.Thr85=
XM_011514468.3:c.254_256delinsCAG	XP_011512770.1:p.Thr85=
XM_017010732.2:c.254_256delinsCAG	XP_016866221.1:p.Thr85=
XR_002956275.1:n.805_807delinsCAG
XR_926136.2:n.803_805delinsCAG
NM_001374747.1:c.254_256delinsCAG	NP_001361676.1:p.Thr85=
NM_145649.5:c.254_256delinsCAG MANE Select	NP_663624.1:p.Thr85=