Canonical Allele Identifier: CA1610029062

Gene: GCNT2

Linked Data

• dbSNP Id: rs1761367396
• gnomAD v4: 6-10529457-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.10529460del , CM000668.2:g.10529460del	GRCh38
NC_000006.11:g.10529693del , CM000668.1:g.10529693del	GRCh37
NC_000006.10:g.10637679del	NCBI36
NG_007469.3:g.42238del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397423.7:n.484+619del
ENST00000495262.7:c.549del MANE Select	ENSP00000419411.2:p.Trp184GlyfsTer14
ENST00000379597.7:c.549del	ENSP00000368917.3:p.Trp184GlyfsTer14
ENST00000397423.6:n.484+619del
ENST00000410107.5:c.67+20302del	ENSP00000386321.1:n.67+20302del
ENST00000474518.1:n.508+619del
ENST00000474983.5:n.1126del
ENST00000475577.5:n.254+1800del
ENST00000483204.1:n.1125del
ENST00000489225.5:n.283+36529del
ENST00000489819.5:n.175+7866del
ENST00000495262.5:c.549del	ENSP00000419411.1:p.Trp184GlyfsTer14
NM_145649.4:c.549del	NP_663624.1:p.Trp184GlyfsTer14
XM_005248999.2:c.318del	XP_005249056.1:p.Trp107GlyfsTer14
XM_006715052.2:c.549del	XP_006715115.1:p.Trp184GlyfsTer14
XM_006715053.2:c.549del	XP_006715116.1:p.Trp184GlyfsTer14
XM_011514465.1:c.549del	XP_011512767.1:p.Trp184GlyfsTer14
XM_011514467.1:c.318del	XP_011512769.1:p.Trp107GlyfsTer14
XM_011514468.1:c.549del	XP_011512770.1:p.Trp184GlyfsTer14
XR_926136.1:n.1100del
XM_006715052.3:c.549del	XP_006715115.1:p.Trp184GlyfsTer14
XM_011514468.3:c.549del	XP_011512770.1:p.Trp184GlyfsTer14
XM_017010732.2:c.549del	XP_016866221.1:p.Trp184GlyfsTer14
XR_002956275.1:n.1100del
XR_926136.2:n.1098del
NM_001374747.1:c.549del	NP_001361676.1:p.Trp184GlyfsTer14
NM_145649.5:c.549del MANE Select	NP_663624.1:p.Trp184GlyfsTer14