Canonical Allele Identifier: CA1610028510

Gene: GCNT2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.10529178_10529181delinsTGAA , CM000668.2:g.10529178_10529181delinsTGAA	GRCh38
NC_000006.11:g.10529411_10529414delinsTGAA , CM000668.1:g.10529411_10529414delinsTGAA	GRCh37
NC_000006.10:g.10637397_10637400delinsTGAA	NCBI36
NG_007469.3:g.41956_41959delinsTGAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397423.7:n.484+337_484+340delinsTGAA
ENST00000483204.2:n.843_846delinsTGAA
ENST00000495262.7:c.267_270delinsTGAA MANE Select	ENSP00000419411.2:p.Ser89=
ENST00000379597.7:c.267_270delinsTGAA	ENSP00000368917.3:p.Ser89=
ENST00000397423.6:n.484+337_484+340delinsTGAA
ENST00000410107.5:c.67+20020_67+20023delinsTGAA	ENSP00000386321.1:n.67+20020_67+20023delinsTGAA
ENST00000474518.1:n.508+337_508+340delinsTGAA
ENST00000474983.5:n.844_847delinsTGAA
ENST00000475577.5:n.254+1518_254+1521delinsTGAA
ENST00000483204.1:n.843_846delinsTGAA
ENST00000489225.5:n.283+36247_283+36250delinsTGAA
ENST00000489819.5:n.175+7584_175+7587delinsTGAA
ENST00000495262.5:c.267_270delinsTGAA	ENSP00000419411.1:p.Ser89=
NM_145649.4:c.267_270delinsTGAA	NP_663624.1:p.Ser89=
XM_005248999.2:c.36_39delinsTGAA	XP_005249056.1:p.Ser12=
XM_006715052.2:c.267_270delinsTGAA	XP_006715115.1:p.Ser89=
XM_006715053.2:c.267_270delinsTGAA	XP_006715116.1:p.Ser89=
XM_011514465.1:c.267_270delinsTGAA	XP_011512767.1:p.Ser89=
XM_011514467.1:c.36_39delinsTGAA	XP_011512769.1:p.Ser12=
XM_011514468.1:c.267_270delinsTGAA	XP_011512770.1:p.Ser89=
XR_926136.1:n.818_821delinsTGAA
XM_006715052.3:c.267_270delinsTGAA	XP_006715115.1:p.Ser89=
XM_011514468.3:c.267_270delinsTGAA	XP_011512770.1:p.Ser89=
XM_017010732.2:c.267_270delinsTGAA	XP_016866221.1:p.Ser89=
XR_002956275.1:n.818_821delinsTGAA
XR_926136.2:n.816_819delinsTGAA
NM_001374747.1:c.267_270delinsTGAA	NP_001361676.1:p.Ser89=
NM_145649.5:c.267_270delinsTGAA MANE Select	NP_663624.1:p.Ser89=