Canonical Allele Identifier: CA1610029399

Gene: GCNT2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.10529603_10529604delinsAC , CM000668.2:g.10529603_10529604delinsAC	GRCh38
NC_000006.11:g.10529836_10529837delinsAC , CM000668.1:g.10529836_10529837delinsAC	GRCh37
NC_000006.10:g.10637822_10637823delinsAC	NCBI36
NG_007469.3:g.42381_42382delinsAC

Transcript Alleles

HGVS	Amino-acid change
ENST00000397423.7:n.484+762_484+763delinsAC
ENST00000495262.7:c.692_693delinsAC MANE Select	ENSP00000419411.2:p.Tyr231=
ENST00000379597.7:c.692_693delinsAC	ENSP00000368917.3:p.Tyr231=
ENST00000397423.6:n.484+762_484+763delinsAC
ENST00000410107.5:c.67+20445_67+20446delinsAC	ENSP00000386321.1:n.67+20445_67+20446deli...
ENST00000474518.1:n.508+762_508+763delinsAC
ENST00000474983.5:n.1269_1270delinsAC
ENST00000475577.5:n.254+1943_254+1944delinsAC
ENST00000483204.1:n.1268_1269delinsAC
ENST00000489225.5:n.283+36672_283+36673delinsAC
ENST00000489819.5:n.175+8009_175+8010delinsAC
ENST00000495262.5:c.692_693delinsAC	ENSP00000419411.1:p.Tyr231=
NM_145649.4:c.692_693delinsAC	NP_663624.1:p.Tyr231=
XM_005248999.2:c.461_462delinsAC	XP_005249056.1:p.Tyr154=
XM_006715052.2:c.692_693delinsAC	XP_006715115.1:p.Tyr231=
XM_006715053.2:c.692_693delinsAC	XP_006715116.1:p.Tyr231=
XM_011514465.1:c.692_693delinsAC	XP_011512767.1:p.Tyr231=
XM_011514467.1:c.461_462delinsAC	XP_011512769.1:p.Tyr154=
XM_011514468.1:c.692_693delinsAC	XP_011512770.1:p.Tyr231=
XR_926136.1:n.1243_1244delinsAC
XM_006715052.3:c.692_693delinsAC	XP_006715115.1:p.Tyr231=
XM_011514468.3:c.692_693delinsAC	XP_011512770.1:p.Tyr231=
XM_017010732.2:c.692_693delinsAC	XP_016866221.1:p.Tyr231=
XR_002956275.1:n.1243_1244delinsAC
XR_926136.2:n.1241_1242delinsAC
NM_001374747.1:c.692_693delinsAC	NP_001361676.1:p.Tyr231=
NM_145649.5:c.692_693delinsAC MANE Select	NP_663624.1:p.Tyr231=