Canonical Allele Identifier: CA362707187
Gene: GCNT2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.10529181A>T , CM000668.2:g.10529181A>T GRCh38
NC_000006.11:g.10529414A>T , CM000668.1:g.10529414A>T GRCh37
NC_000006.10:g.10637400A>T NCBI36
NG_007469.3:g.41959A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000397423.7:n.484+340A>T
ENST00000483204.2:n.846A>T
ENST00000495262.7:c.270A>T MANE Select ENSP00000419411.2:p.Glu90Asp
ENST00000379597.7:c.270A>T ENSP00000368917.3:p.Glu90Asp
ENST00000397423.6:n.484+340A>T
ENST00000410107.5:c.67+20023A>T ENSP00000386321.1:n.67+20023A>T
ENST00000474518.1:n.508+340A>T
ENST00000474983.5:n.847A>T
ENST00000475577.5:n.254+1521A>T
ENST00000483204.1:n.846A>T
ENST00000489225.5:n.283+36250A>T
ENST00000489819.5:n.175+7587A>T
ENST00000495262.5:c.270A>T ENSP00000419411.1:p.Glu90Asp
NM_145649.4:c.270A>T NP_663624.1:p.Glu90Asp
XM_005248999.2:c.39A>T XP_005249056.1:p.Glu13Asp
XM_006715052.2:c.270A>T XP_006715115.1:p.Glu90Asp
XM_006715053.2:c.270A>T XP_006715116.1:p.Glu90Asp
XM_011514465.1:c.270A>T XP_011512767.1:p.Glu90Asp
XM_011514467.1:c.39A>T XP_011512769.1:p.Glu13Asp
XM_011514468.1:c.270A>T XP_011512770.1:p.Glu90Asp
XR_926136.1:n.821A>T
XM_006715052.3:c.270A>T XP_006715115.1:p.Glu90Asp
XM_011514468.3:c.270A>T XP_011512770.1:p.Glu90Asp
XM_017010732.2:c.270A>T XP_016866221.1:p.Glu90Asp
XR_002956275.1:n.821A>T
XR_926136.2:n.819A>T
NM_001374747.1:c.270A>T NP_001361676.1:p.Glu90Asp
NM_145649.5:c.270A>T MANE Select NP_663624.1:p.Glu90Asp