Canonical Allele Identifier: CA1610029159

Gene: GCNT2

Linked Data

• dbSNP Id: rs1198815799
• gnomAD v4: 6-10529493-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.10529496del , CM000668.2:g.10529496del	GRCh38
NC_000006.11:g.10529729del , CM000668.1:g.10529729del	GRCh37
NC_000006.10:g.10637715del	NCBI36
NG_007469.3:g.42274del

Transcript Alleles

HGVS	Amino-acid change
ENST00000397423.7:n.484+655del
ENST00000495262.7:c.585del MANE Select	ENSP00000419411.2:p.Leu197Ter
ENST00000379597.7:c.585del	ENSP00000368917.3:p.Leu197Ter
ENST00000397423.6:n.484+655del
ENST00000410107.5:c.67+20338del	ENSP00000386321.1:n.67+20338del
ENST00000474518.1:n.508+655del
ENST00000474983.5:n.1162del
ENST00000475577.5:n.254+1836del
ENST00000483204.1:n.1161del
ENST00000489225.5:n.283+36565del
ENST00000489819.5:n.175+7902del
ENST00000495262.5:c.585del	ENSP00000419411.1:p.Leu197Ter
NM_145649.4:c.585del	NP_663624.1:p.Leu197Ter
XM_005248999.2:c.354del	XP_005249056.1:p.Leu120Ter
XM_006715052.2:c.585del	XP_006715115.1:p.Leu197Ter
XM_006715053.2:c.585del	XP_006715116.1:p.Leu197Ter
XM_011514465.1:c.585del	XP_011512767.1:p.Leu197Ter
XM_011514467.1:c.354del	XP_011512769.1:p.Leu120Ter
XM_011514468.1:c.585del	XP_011512770.1:p.Leu197Ter
XR_926136.1:n.1136del
XM_006715052.3:c.585del	XP_006715115.1:p.Leu197Ter
XM_011514468.3:c.585del	XP_011512770.1:p.Leu197Ter
XM_017010732.2:c.585del	XP_016866221.1:p.Leu197Ter
XR_002956275.1:n.1136del
XR_926136.2:n.1134del
NM_001374747.1:c.585del	NP_001361676.1:p.Leu197Ter
NM_145649.5:c.585del MANE Select	NP_663624.1:p.Leu197Ter