Canonical Allele Identifier: CA2428428857
Gene: SLC35A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.48905066G= , CM000685.2:g.48905066G= GRCh38
NC_000023.10:g.48762343G= , CM000685.1:g.48762343G= GRCh37
NC_000023.9:g.48647287G= NCBI36
NG_015967.1:g.12149G=
NG_034300.1:g.11893C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000247138.11:c.843C= MANE Select ENSP00000247138.5:p.Gly281=
ENST00000247138.10:c.843C= ENSP00000247138.5:p.Gly281=
ENST00000376515.8:c.355-174C= ENSP00000365698.3:n.355-174C=
ENST00000376521.6:c.843C= ENSP00000365704.1:p.Gly281=
ENST00000376529.8:c.427-174C= ENSP00000365712.3:n.427-174C=
ENST00000413561.7:c.405C=
ENST00000445167.7:c.427-174C= ENSP00000402726.2:n.427-174C=
ENST00000452555.7:c.927C= ENSP00000416002.2:p.Gly309=
ENST00000616181.5:c.882C= ENSP00000478617.1:p.Gly294=
ENST00000635285.1:c.843C= ENSP00000489484.1:p.Gly281=
ENST00000635460.1:c.424+1326C=
ENST00000635589.1:c.660C= ENSP00000489197.1:p.Gly220=
ENST00000635628.1:c.*737C= ENSP00000489613.1:n.*737C=
NM_001032289.2:c.427-174C= NP_001027460.1:n.427-174C=
NM_001042498.2:c.843C= NP_001035963.1:p.Gly281=
NM_001282647.1:c.427-174C= NP_001269576.1:n.427-174C=
NM_001282648.1:c.355-174C= NP_001269577.1:n.355-174C=
NM_001282649.1:c.660C= NP_001269578.1:p.Gly220=
NM_001282650.1:c.882C= NP_001269579.1:p.Gly294=
NM_001282651.1:c.927C= NP_001269580.1:p.Gly309=
NM_005660.2:c.843C= NP_005651.1:p.Gly281=
NM_005660.3:c.843C= MANE Select NP_005651.1:p.Gly281=
NM_001032289.3:c.427-174C= NP_001027460.1:n.427-174C=
NM_001042498.3:c.843C= NP_001035963.1:p.Gly281=
NM_001282647.2:c.427-174C= NP_001269576.1:n.427-174C=
NM_001282649.2:c.660C= NP_001269578.1:p.Gly220=
NM_001282650.2:c.882C= NP_001269579.1:p.Gly294=
NM_001282651.2:c.927C= NP_001269580.1:p.Gly309=
NM_001282648.2:c.355-174C= NP_001269577.1:n.355-174C=