Canonical Allele Identifier: CA1610029480

Gene: GCNT2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.10529665_10529668delinsACTC , CM000668.2:g.10529665_10529668delinsACTC	GRCh38
NC_000006.11:g.10529898_10529901delinsACTC , CM000668.1:g.10529898_10529901delinsACTC	GRCh37
NC_000006.10:g.10637884_10637887delinsACTC	NCBI36
NG_007469.3:g.42443_42446delinsACTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397423.7:n.484+824_484+827delinsACTC
ENST00000495262.7:c.754_757delinsACTC MANE Select	ENSP00000419411.2:p.Thr252=
ENST00000379597.7:c.754_757delinsACTC	ENSP00000368917.3:p.Thr252=
ENST00000397423.6:n.484+824_484+827delinsACTC
ENST00000410107.5:c.67+20507_67+20510delinsACTC	ENSP00000386321.1:n.67+20507_67+20510delinsACTC
ENST00000474518.1:n.508+824_508+827delinsACTC
ENST00000474983.5:n.1331_1334delinsACTC
ENST00000475577.5:n.254+2005_254+2008delinsACTC
ENST00000483204.1:n.1330_1333delinsACTC
ENST00000489225.5:n.283+36734_283+36737delinsACTC
ENST00000489819.5:n.175+8071_175+8074delinsACTC
ENST00000495262.5:c.754_757delinsACTC	ENSP00000419411.1:p.Thr252=
NM_145649.4:c.754_757delinsACTC	NP_663624.1:p.Thr252=
XM_005248999.2:c.523_526delinsACTC	XP_005249056.1:p.Thr175=
XM_006715052.2:c.754_757delinsACTC	XP_006715115.1:p.Thr252=
XM_006715053.2:c.754_757delinsACTC	XP_006715116.1:p.Thr252=
XM_011514465.1:c.754_757delinsACTC	XP_011512767.1:p.Thr252=
XM_011514467.1:c.523_526delinsACTC	XP_011512769.1:p.Thr175=
XM_011514468.1:c.754_757delinsACTC	XP_011512770.1:p.Thr252=
XR_926136.1:n.1305_1308delinsACTC
XM_006715052.3:c.754_757delinsACTC	XP_006715115.1:p.Thr252=
XM_011514468.3:c.754_757delinsACTC	XP_011512770.1:p.Thr252=
XM_017010732.2:c.754_757delinsACTC	XP_016866221.1:p.Thr252=
XR_002956275.1:n.1305_1308delinsACTC
XR_926136.2:n.1303_1306delinsACTC
NM_001374747.1:c.754_757delinsACTC	NP_001361676.1:p.Thr252=
NM_145649.5:c.754_757delinsACTC MANE Select	NP_663624.1:p.Thr252=