Canonical Allele Identifier: CA1610028530

Gene: GCNT2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.10529194_10529208delinsTTCCCTTTAGCTTAC , CM000668.2:g.10529194_10529208delinsTTCCCTTTAGCTTAC	GRCh38
NC_000006.11:g.10529427_10529441delinsTTCCCTTTAGCTTAC , CM000668.1:g.10529427_10529441delinsTTCCCTTTAGCTTAC	GRCh37
NC_000006.10:g.10637413_10637427delinsTTCCCTTTAGCTTAC	NCBI36
NG_007469.3:g.41972_41986delinsTTCCCTTTAGCTTAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397423.7:n.484+353_484+367delinsTTCCCTTTAGCTTAC
ENST00000483204.2:n.859_873delinsTTCCCTTTAGCTTAC
ENST00000495262.7:c.283_297delinsTTCCCTTTAGCTTAC MANE Select	ENSP00000419411.2:p.Phe95=
ENST00000379597.7:c.283_297delinsTTCCCTTTAGCTTAC	ENSP00000368917.3:p.Phe95=
ENST00000397423.6:n.484+353_484+367delinsTTCCCTTTAGCTTAC
ENST00000410107.5:c.67+20036_67+20050delinsTTCCCTTTAGCTTAC	ENSP00000386321.1:n.67+20036_67+20050delinsTTCCCTTTAGCTTAC
ENST00000474518.1:n.508+353_508+367delinsTTCCCTTTAGCTTAC
ENST00000474983.5:n.860_874delinsTTCCCTTTAGCTTAC
ENST00000475577.5:n.254+1534_254+1548delinsTTCCCTTTAGCTTAC
ENST00000483204.1:n.859_873delinsTTCCCTTTAGCTTAC
ENST00000489225.5:n.283+36263_283+36277delinsTTCCCTTTAGCTTAC
ENST00000489819.5:n.175+7600_175+7614delinsTTCCCTTTAGCTTAC
ENST00000495262.5:c.283_297delinsTTCCCTTTAGCTTAC	ENSP00000419411.1:p.Phe95=
NM_145649.4:c.283_297delinsTTCCCTTTAGCTTAC	NP_663624.1:p.Phe95=
XM_005248999.2:c.52_66delinsTTCCCTTTAGCTTAC	XP_005249056.1:p.Phe18=
XM_006715052.2:c.283_297delinsTTCCCTTTAGCTTAC	XP_006715115.1:p.Phe95=
XM_006715053.2:c.283_297delinsTTCCCTTTAGCTTAC	XP_006715116.1:p.Phe95=
XM_011514465.1:c.283_297delinsTTCCCTTTAGCTTAC	XP_011512767.1:p.Phe95=
XM_011514467.1:c.52_66delinsTTCCCTTTAGCTTAC	XP_011512769.1:p.Phe18=
XM_011514468.1:c.283_297delinsTTCCCTTTAGCTTAC	XP_011512770.1:p.Phe95=
XR_926136.1:n.834_848delinsTTCCCTTTAGCTTAC
XM_006715052.3:c.283_297delinsTTCCCTTTAGCTTAC	XP_006715115.1:p.Phe95=
XM_011514468.3:c.283_297delinsTTCCCTTTAGCTTAC	XP_011512770.1:p.Phe95=
XM_017010732.2:c.283_297delinsTTCCCTTTAGCTTAC	XP_016866221.1:p.Phe95=
XR_002956275.1:n.834_848delinsTTCCCTTTAGCTTAC
XR_926136.2:n.832_846delinsTTCCCTTTAGCTTAC
NM_001374747.1:c.283_297delinsTTCCCTTTAGCTTAC	NP_001361676.1:p.Phe95=
NM_145649.5:c.283_297delinsTTCCCTTTAGCTTAC MANE Select	NP_663624.1:p.Phe95=