Canonical Allele Identifier: CA1610028853

Gene: GCNT2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.10529373_10529376delinsCAAG , CM000668.2:g.10529373_10529376delinsCAAG	GRCh38
NC_000006.11:g.10529606_10529609delinsCAAG , CM000668.1:g.10529606_10529609delinsCAAG	GRCh37
NC_000006.10:g.10637592_10637595delinsCAAG	NCBI36
NG_007469.3:g.42151_42154delinsCAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397423.7:n.484+532_484+535delinsCAAG
ENST00000495262.7:c.462_465delinsCAAG MANE Select	ENSP00000419411.2:p.Ser154=
ENST00000379597.7:c.462_465delinsCAAG	ENSP00000368917.3:p.Ser154=
ENST00000397423.6:n.484+532_484+535delinsCAAG
ENST00000410107.5:c.67+20215_67+20218delinsCAAG	ENSP00000386321.1:n.67+20215_67+20218delinsCAAG
ENST00000474518.1:n.508+532_508+535delinsCAAG
ENST00000474983.5:n.1039_1042delinsCAAG
ENST00000475577.5:n.254+1713_254+1716delinsCAAG
ENST00000483204.1:n.1038_1041delinsCAAG
ENST00000489225.5:n.283+36442_283+36445delinsCAAG
ENST00000489819.5:n.175+7779_175+7782delinsCAAG
ENST00000495262.5:c.462_465delinsCAAG	ENSP00000419411.1:p.Ser154=
NM_145649.4:c.462_465delinsCAAG	NP_663624.1:p.Ser154=
XM_005248999.2:c.231_234delinsCAAG	XP_005249056.1:p.Ser77=
XM_006715052.2:c.462_465delinsCAAG	XP_006715115.1:p.Ser154=
XM_006715053.2:c.462_465delinsCAAG	XP_006715116.1:p.Ser154=
XM_011514465.1:c.462_465delinsCAAG	XP_011512767.1:p.Ser154=
XM_011514467.1:c.231_234delinsCAAG	XP_011512769.1:p.Ser77=
XM_011514468.1:c.462_465delinsCAAG	XP_011512770.1:p.Ser154=
XR_926136.1:n.1013_1016delinsCAAG
XM_006715052.3:c.462_465delinsCAAG	XP_006715115.1:p.Ser154=
XM_011514468.3:c.462_465delinsCAAG	XP_011512770.1:p.Ser154=
XM_017010732.2:c.462_465delinsCAAG	XP_016866221.1:p.Ser154=
XR_002956275.1:n.1013_1016delinsCAAG
XR_926136.2:n.1011_1014delinsCAAG
NM_001374747.1:c.462_465delinsCAAG	NP_001361676.1:p.Ser154=
NM_145649.5:c.462_465delinsCAAG MANE Select	NP_663624.1:p.Ser154=