Canonical Allele Identifier: CA2428428710
Gene: SLC35A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.48904642G= , CM000685.2:g.48904642G= GRCh38
NC_000023.10:g.48761919G= , CM000685.1:g.48761919G= GRCh37
NC_000023.9:g.48646863G= NCBI36
NG_015967.1:g.11725G=
NG_034300.1:g.12317C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000247138.11:c.1163+104C= MANE Select ENSP00000247138.5:n.1163+104C=
ENST00000247138.10:c.1163+104C= ENSP00000247138.5:n.1163+104C=
ENST00000376515.8:c.605C= ENSP00000365698.3:p.Pro202=
ENST00000376521.6:c.*85C= ENSP00000365704.1:n.*85C=
ENST00000376529.8:c.573+104C= ENSP00000365712.3:n.573+104C=
ENST00000413561.7:c.829C=
ENST00000445167.7:c.677C= ENSP00000402726.2:p.Pro226=
ENST00000452555.7:c.*85C= ENSP00000416002.2:n.*85C=
ENST00000616181.5:c.*85C= ENSP00000478617.1:n.*85C=
ENST00000635285.1:c.*85C= ENSP00000489484.1:n.*85C=
ENST00000635460.1:c.425-1177C=
ENST00000635589.1:c.*85C= ENSP00000489197.1:n.*85C=
ENST00000635628.1:c.*1161C= ENSP00000489613.1:n.*1161C=
NM_001032289.2:c.677C= NP_001027460.1:p.Pro226=
NM_001042498.2:c.*85C= NP_001035963.1:n.*85C=
NM_001282647.1:c.573+104C= NP_001269576.1:n.573+104C=
NM_001282648.1:c.605C= NP_001269577.1:p.Pro202=
NM_001282649.1:c.*85C= NP_001269578.1:n.*85C=
NM_001282650.1:c.*85C= NP_001269579.1:n.*85C=
NM_001282651.1:c.*85C= NP_001269580.1:n.*85C=
NM_005660.2:c.1163+104C= NP_005651.1:n.1163+104C=
NM_005660.3:c.1163+104C= MANE Select NP_005651.1:n.1163+104C=
NM_001032289.3:c.677C= NP_001027460.1:p.Pro226=
NM_001042498.3:c.*85C= NP_001035963.1:n.*85C=
NM_001282647.2:c.573+104C= NP_001269576.1:n.573+104C=
NM_001282649.2:c.*85C= NP_001269578.1:n.*85C=
NM_001282650.2:c.*85C= NP_001269579.1:n.*85C=
NM_001282651.2:c.*85C= NP_001269580.1:n.*85C=
NM_001282648.2:c.605C= NP_001269577.1:p.Pro202=