Canonical Allele Identifier: CA1610028924
Gene: GCNT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.10529399G= , CM000668.2:g.10529399G= GRCh38
NC_000006.11:g.10529632G= , CM000668.1:g.10529632G= GRCh37
NC_000006.10:g.10637618G= NCBI36
NG_007469.3:g.42177G=

Transcript Alleles

HGVS Amino-acid change
ENST00000397423.7:n.484+558G=
ENST00000495262.7:c.488G= MANE Select ENSP00000419411.2:p.Gly163=
ENST00000379597.7:c.488G= ENSP00000368917.3:p.Gly163=
ENST00000397423.6:n.484+558G=
ENST00000410107.5:c.67+20241G= ENSP00000386321.1:n.67+20241G=
ENST00000474518.1:n.508+558G=
ENST00000474983.5:n.1065G=
ENST00000475577.5:n.254+1739G=
ENST00000483204.1:n.1064G=
ENST00000489225.5:n.283+36468G=
ENST00000489819.5:n.175+7805G=
ENST00000495262.5:c.488G= ENSP00000419411.1:p.Gly163=
NM_145649.4:c.488G= NP_663624.1:p.Gly163=
XM_005248999.2:c.257G= XP_005249056.1:p.Gly86=
XM_006715052.2:c.488G= XP_006715115.1:p.Gly163=
XM_006715053.2:c.488G= XP_006715116.1:p.Gly163=
XM_011514465.1:c.488G= XP_011512767.1:p.Gly163=
XM_011514467.1:c.257G= XP_011512769.1:p.Gly86=
XM_011514468.1:c.488G= XP_011512770.1:p.Gly163=
XR_926136.1:n.1039G=
XM_006715052.3:c.488G= XP_006715115.1:p.Gly163=
XM_011514468.3:c.488G= XP_011512770.1:p.Gly163=
XM_017010732.2:c.488G= XP_016866221.1:p.Gly163=
XR_002956275.1:n.1039G=
XR_926136.2:n.1037G=
NM_001374747.1:c.488G= NP_001361676.1:p.Gly163=
NM_145649.5:c.488G= MANE Select NP_663624.1:p.Gly163=