Canonical Allele Identifier: CA2693665032
Gene: SLC35A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.48904592_48904593del , CM000685.2:g.48904592_48904593del GRCh38
NC_000023.10:g.48761869_48761870del , CM000685.1:g.48761869_48761870del GRCh37
NC_000023.9:g.48646813_48646814del NCBI36
NG_015967.1:g.11675_11676del
NG_034300.1:g.12366_12367del

Transcript Alleles

HGVS Amino-acid Change
ENST00000247138.11:c.1163+153_1163+154del MANE Select ENSP00000247138.5:n.1163+153_1163+154del
ENST00000247138.10:c.1163+153_1163+154del ENSP00000247138.5:n.1163+153_1163+154del
ENST00000376515.8:c.654_655del ENSP00000365698.3:p.His218GlnfsTer20
ENST00000376521.6:c.*134_*135del ENSP00000365704.1:n.*134_*135del
ENST00000376529.8:c.573+153_573+154del ENSP00000365712.3:n.573+153_573+154del
ENST00000413561.7:c.878_879del
ENST00000445167.7:c.726_727del ENSP00000402726.2:p.His242GlnfsTer20
ENST00000452555.7:c.*134_*135del ENSP00000416002.2:n.*134_*135del
ENST00000616181.5:c.*134_*135del ENSP00000478617.1:n.*134_*135del
ENST00000635285.1:c.*134_*135del ENSP00000489484.1:n.*134_*135del
ENST00000635460.1:c.425-1128_425-1127del
ENST00000635589.1:c.*134_*135del ENSP00000489197.1:n.*134_*135del
ENST00000635628.1:c.*1210_*1211del ENSP00000489613.1:n.*1210_*1211del
NM_001032289.2:c.726_727del NP_001027460.1:p.His242GlnfsTer20
NM_001042498.2:c.*134_*135del NP_001035963.1:n.*134_*135del
NM_001282647.1:c.573+153_573+154del NP_001269576.1:n.573+153_573+154del
NM_001282648.1:c.654_655del NP_001269577.1:p.His218GlnfsTer20
NM_001282649.1:c.*134_*135del NP_001269578.1:n.*134_*135del
NM_001282650.1:c.*134_*135del NP_001269579.1:n.*134_*135del
NM_001282651.1:c.*134_*135del NP_001269580.1:n.*134_*135del
NM_005660.2:c.1163+153_1163+154del NP_005651.1:n.1163+153_1163+154del
NM_005660.3:c.1163+153_1163+154del MANE Select NP_005651.1:n.1163+153_1163+154del
NM_001032289.3:c.726_727del NP_001027460.1:p.His242GlnfsTer20
NM_001042498.3:c.*134_*135del NP_001035963.1:n.*134_*135del
NM_001282647.2:c.573+153_573+154del NP_001269576.1:n.573+153_573+154del
NM_001282649.2:c.*134_*135del NP_001269578.1:n.*134_*135del
NM_001282650.2:c.*134_*135del NP_001269579.1:n.*134_*135del
NM_001282651.2:c.*134_*135del NP_001269580.1:n.*134_*135del
NM_001282648.2:c.654_655del NP_001269577.1:p.His218GlnfsTer20