Canonical Allele Identifier: CA1610029445

Gene: GCNT2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.10529646_10529647delinsTA , CM000668.2:g.10529646_10529647delinsTA	GRCh38
NC_000006.11:g.10529879_10529880delinsTA , CM000668.1:g.10529879_10529880delinsTA	GRCh37
NC_000006.10:g.10637865_10637866delinsTA	NCBI36
NG_007469.3:g.42424_42425delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397423.7:n.484+805_484+806delinsTA
ENST00000495262.7:c.735_736delinsTA MANE Select	ENSP00000419411.2:p.Ile245=
ENST00000379597.7:c.735_736delinsTA	ENSP00000368917.3:p.Ile245=
ENST00000397423.6:n.484+805_484+806delinsTA
ENST00000410107.5:c.67+20488_67+20489delinsTA	ENSP00000386321.1:n.67+20488_67+20489delinsTA
ENST00000474518.1:n.508+805_508+806delinsTA
ENST00000474983.5:n.1312_1313delinsTA
ENST00000475577.5:n.254+1986_254+1987delinsTA
ENST00000483204.1:n.1311_1312delinsTA
ENST00000489225.5:n.283+36715_283+36716delinsTA
ENST00000489819.5:n.175+8052_175+8053delinsTA
ENST00000495262.5:c.735_736delinsTA	ENSP00000419411.1:p.Ile245=
NM_145649.4:c.735_736delinsTA	NP_663624.1:p.Ile245=
XM_005248999.2:c.504_505delinsTA	XP_005249056.1:p.Ile168=
XM_006715052.2:c.735_736delinsTA	XP_006715115.1:p.Ile245=
XM_006715053.2:c.735_736delinsTA	XP_006715116.1:p.Ile245=
XM_011514465.1:c.735_736delinsTA	XP_011512767.1:p.Ile245=
XM_011514467.1:c.504_505delinsTA	XP_011512769.1:p.Ile168=
XM_011514468.1:c.735_736delinsTA	XP_011512770.1:p.Ile245=
XR_926136.1:n.1286_1287delinsTA
XM_006715052.3:c.735_736delinsTA	XP_006715115.1:p.Ile245=
XM_011514468.3:c.735_736delinsTA	XP_011512770.1:p.Ile245=
XM_017010732.2:c.735_736delinsTA	XP_016866221.1:p.Ile245=
XR_002956275.1:n.1286_1287delinsTA
XR_926136.2:n.1284_1285delinsTA
NM_001374747.1:c.735_736delinsTA	NP_001361676.1:p.Ile245=
NM_145649.5:c.735_736delinsTA MANE Select	NP_663624.1:p.Ile245=