Canonical Allele Identifier: CA2536008977

Gene: GCNT2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.10529220_10529221insATT , CM000668.2:g.10529220_10529221insATT	GRCh38
NC_000006.11:g.10529453_10529454insATT , CM000668.1:g.10529453_10529454insATT	GRCh37
NC_000006.10:g.10637439_10637440insATT	NCBI36
NG_007469.3:g.41998_41999insATT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397423.7:n.484+379_484+380insATT
ENST00000483204.2:n.885_886insATT
ENST00000495262.7:c.309_310insATT MANE Select	ENSP00000419411.2:p.Ile103_His104insIle
ENST00000379597.7:c.309_310insATT	ENSP00000368917.3:p.Ile103_His104insIle
ENST00000397423.6:n.484+379_484+380insATT
ENST00000410107.5:c.67+20062_67+20063insATT	ENSP00000386321.1:n.67+20062_67+20063insATT
ENST00000474518.1:n.508+379_508+380insATT
ENST00000474983.5:n.886_887insATT
ENST00000475577.5:n.254+1560_254+1561insATT
ENST00000483204.1:n.885_886insATT
ENST00000489225.5:n.283+36289_283+36290insATT
ENST00000489819.5:n.175+7626_175+7627insATT
ENST00000495262.5:c.309_310insATT	ENSP00000419411.1:p.Ile103_His104insIle
NM_145649.4:c.309_310insATT	NP_663624.1:p.Ile103_His104insIle
XM_005248999.2:c.78_79insATT	XP_005249056.1:p.Ile26_His27insIle
XM_006715052.2:c.309_310insATT	XP_006715115.1:p.Ile103_His104insIle
XM_006715053.2:c.309_310insATT	XP_006715116.1:p.Ile103_His104insIle
XM_011514465.1:c.309_310insATT	XP_011512767.1:p.Ile103_His104insIle
XM_011514467.1:c.78_79insATT	XP_011512769.1:p.Ile26_His27insIle
XM_011514468.1:c.309_310insATT	XP_011512770.1:p.Ile103_His104insIle
XR_926136.1:n.860_861insATT
XM_006715052.3:c.309_310insATT	XP_006715115.1:p.Ile103_His104insIle
XM_011514468.3:c.309_310insATT	XP_011512770.1:p.Ile103_His104insIle
XM_017010732.2:c.309_310insATT	XP_016866221.1:p.Ile103_His104insIle
XR_002956275.1:n.860_861insATT
XR_926136.2:n.858_859insATT
NM_001374747.1:c.309_310insATT	NP_001361676.1:p.Ile103_His104insIle
NM_145649.5:c.309_310insATT MANE Select	NP_663624.1:p.Ile103_His104insIle