Canonical Allele Identifier: CA2769966104

Gene: GCNT2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.10529790_10529791insCAA , CM000668.2:g.10529790_10529791insCAA	GRCh38
NC_000006.11:g.10530023_10530024insCAA , CM000668.1:g.10530023_10530024insCAA	GRCh37
NC_000006.10:g.10638009_10638010insCAA	NCBI36
NG_007469.3:g.42568_42569insCAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397423.7:n.484+949_484+950insCAA
ENST00000495262.7:c.879_880insCAA MANE Select	ENSP00000419411.2:p.Thr293_Tyr294insGln
ENST00000379597.7:c.879_880insCAA	ENSP00000368917.3:p.Thr293_Tyr294insGln
ENST00000397423.6:n.484+949_484+950insCAA
ENST00000410107.5:c.67+20632_67+20633insCAA	ENSP00000386321.1:n.67+20632_67+20633insCAA
ENST00000474518.1:n.508+949_508+950insCAA
ENST00000474983.5:n.1456_1457insCAA
ENST00000475577.5:n.254+2130_254+2131insCAA
ENST00000483204.1:n.1455_1456insCAA
ENST00000489225.5:n.283+36859_283+36860insCAA
ENST00000489819.5:n.175+8196_175+8197insCAA
ENST00000495262.5:c.879_880insCAA	ENSP00000419411.1:p.Thr293_Tyr294insGln
NM_145649.4:c.879_880insCAA	NP_663624.1:p.Thr293_Tyr294insGln
XM_005248999.2:c.648_649insCAA	XP_005249056.1:p.Thr216_Tyr217insGln
XM_006715052.2:c.879_880insCAA	XP_006715115.1:p.Thr293_Tyr294insGln
XM_006715053.2:c.879_880insCAA	XP_006715116.1:p.Thr293_Tyr294insGln
XM_011514465.1:c.879_880insCAA	XP_011512767.1:p.Thr293_Tyr294insGln
XM_011514467.1:c.648_649insCAA	XP_011512769.1:p.Thr216_Tyr217insGln
XM_011514468.1:c.879_880insCAA	XP_011512770.1:p.Thr293_Tyr294insGln
XR_926136.1:n.1430_1431insCAA
XM_006715052.3:c.879_880insCAA	XP_006715115.1:p.Thr293_Tyr294insGln
XM_011514468.3:c.879_880insCAA	XP_011512770.1:p.Thr293_Tyr294insGln
XM_017010732.2:c.879_880insCAA	XP_016866221.1:p.Thr293_Tyr294insGln
XR_002956275.1:n.1430_1431insCAA
XR_926136.2:n.1428_1429insCAA
NM_001374747.1:c.879_880insCAA	NP_001361676.1:p.Thr293_Tyr294insGln
NM_145649.5:c.879_880insCAA MANE Select	NP_663624.1:p.Thr293_Tyr294insGln