Canonical Allele Identifier: CA1610028489

Gene: GCNT2

Linked Data

• dbSNP Id: rs1761347252

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.10529167_10529168del , CM000668.2:g.10529167_10529168del	GRCh38
NC_000006.11:g.10529400_10529401del , CM000668.1:g.10529400_10529401del	GRCh37
NC_000006.10:g.10637386_10637387del	NCBI36
NG_007469.3:g.41945_41946del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397423.7:n.484+326_484+327del
ENST00000483204.2:n.832_833del
ENST00000495262.7:c.256_257del MANE Select	ENSP00000419411.2:p.Glu86AsnfsTer4
ENST00000379597.7:c.256_257del	ENSP00000368917.3:p.Glu86AsnfsTer4
ENST00000397423.6:n.484+326_484+327del
ENST00000410107.5:c.67+20009_67+20010del	ENSP00000386321.1:n.67+20009_67+20010del
ENST00000474518.1:n.508+326_508+327del
ENST00000474983.5:n.833_834del
ENST00000475577.5:n.254+1507_254+1508del
ENST00000483204.1:n.832_833del
ENST00000489225.5:n.283+36236_283+36237del
ENST00000489819.5:n.175+7573_175+7574del
ENST00000495262.5:c.256_257del	ENSP00000419411.1:p.Glu86AsnfsTer4
NM_145649.4:c.256_257del	NP_663624.1:p.Glu86AsnfsTer4
XM_005248999.2:c.25_26del	XP_005249056.1:p.Glu9AsnfsTer4
XM_006715052.2:c.256_257del	XP_006715115.1:p.Glu86AsnfsTer4
XM_006715053.2:c.256_257del	XP_006715116.1:p.Glu86AsnfsTer4
XM_011514465.1:c.256_257del	XP_011512767.1:p.Glu86AsnfsTer4
XM_011514467.1:c.25_26del	XP_011512769.1:p.Glu9AsnfsTer4
XM_011514468.1:c.256_257del	XP_011512770.1:p.Glu86AsnfsTer4
XR_926136.1:n.807_808del
XM_006715052.3:c.256_257del	XP_006715115.1:p.Glu86AsnfsTer4
XM_011514468.3:c.256_257del	XP_011512770.1:p.Glu86AsnfsTer4
XM_017010732.2:c.256_257del	XP_016866221.1:p.Glu86AsnfsTer4
XR_002956275.1:n.807_808del
XR_926136.2:n.805_806del
NM_001374747.1:c.256_257del	NP_001361676.1:p.Glu86AsnfsTer4
NM_145649.5:c.256_257del MANE Select	NP_663624.1:p.Glu86AsnfsTer4