Canonical Allele Identifier: CA1610028938

Gene: GCNT2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.10529402_10529409delinsTCTCCAGG , CM000668.2:g.10529402_10529409delinsTCTCCAGG	GRCh38
NC_000006.11:g.10529635_10529642delinsTCTCCAGG , CM000668.1:g.10529635_10529642delinsTCTCCAGG	GRCh37
NC_000006.10:g.10637621_10637628delinsTCTCCAGG	NCBI36
NG_007469.3:g.42180_42187delinsTCTCCAGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397423.7:n.484+561_484+568delinsTCTCCAGG
ENST00000495262.7:c.491_498delinsTCTCCAGG MANE Select	ENSP00000419411.2:p.Ile164=
ENST00000379597.7:c.491_498delinsTCTCCAGG	ENSP00000368917.3:p.Ile164=
ENST00000397423.6:n.484+561_484+568delinsTCTCCAGG
ENST00000410107.5:c.67+20244_67+20251delinsTCTCCAGG	ENSP00000386321.1:n.67+20244_67+20251delinsTCTCCAGG
ENST00000474518.1:n.508+561_508+568delinsTCTCCAGG
ENST00000474983.5:n.1068_1075delinsTCTCCAGG
ENST00000475577.5:n.254+1742_254+1749delinsTCTCCAGG
ENST00000483204.1:n.1067_1074delinsTCTCCAGG
ENST00000489225.5:n.283+36471_283+36478delinsTCTCCAGG
ENST00000489819.5:n.175+7808_175+7815delinsTCTCCAGG
ENST00000495262.5:c.491_498delinsTCTCCAGG	ENSP00000419411.1:p.Ile164=
NM_145649.4:c.491_498delinsTCTCCAGG	NP_663624.1:p.Ile164=
XM_005248999.2:c.260_267delinsTCTCCAGG	XP_005249056.1:p.Ile87=
XM_006715052.2:c.491_498delinsTCTCCAGG	XP_006715115.1:p.Ile164=
XM_006715053.2:c.491_498delinsTCTCCAGG	XP_006715116.1:p.Ile164=
XM_011514465.1:c.491_498delinsTCTCCAGG	XP_011512767.1:p.Ile164=
XM_011514467.1:c.260_267delinsTCTCCAGG	XP_011512769.1:p.Ile87=
XM_011514468.1:c.491_498delinsTCTCCAGG	XP_011512770.1:p.Ile164=
XR_926136.1:n.1042_1049delinsTCTCCAGG
XM_006715052.3:c.491_498delinsTCTCCAGG	XP_006715115.1:p.Ile164=
XM_011514468.3:c.491_498delinsTCTCCAGG	XP_011512770.1:p.Ile164=
XM_017010732.2:c.491_498delinsTCTCCAGG	XP_016866221.1:p.Ile164=
XR_002956275.1:n.1042_1049delinsTCTCCAGG
XR_926136.2:n.1040_1047delinsTCTCCAGG
NM_001374747.1:c.491_498delinsTCTCCAGG	NP_001361676.1:p.Ile164=
NM_145649.5:c.491_498delinsTCTCCAGG MANE Select	NP_663624.1:p.Ile164=