Canonical Allele Identifier: CA2840294699
Gene: SLC35E3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.68746470dup , CM000674.2:g.68746470dup GRCh38
NC_000012.11:g.69140250dup , CM000674.1:g.69140250dup GRCh37
NC_000012.10:g.67426517dup NCBI36
NG_046600.2:g.64520dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000319429.7:n.336dup
ENST00000398004.4:c.93dup MANE Select ENSP00000381089.2:p.Asn32GlnfsTer?
ENST00000673712.1:c.93dup ENSP00000501065.1:p.Asn32GlnfsTer?
ENST00000674096.1:c.93dup ENSP00000501130.1:p.Asn32GlnfsTer?
ENST00000398004.3:c.93dup ENSP00000381089.2:p.Asn32GlnfsTer?
NM_018656.2:c.93dup NP_061126.2:p.Asn32GlnfsTer?
XM_005269006.2:c.93dup XP_005269063.1:p.Asn32GlnfsTer?
NM_001354997.1:c.93dup NP_001341926.1:p.Asn32GlnfsTer?
NM_001354998.1:c.93dup NP_001341927.1:p.Asn32GlnfsTer?
NM_018656.3:c.93dup NP_061126.2:p.Asn32GlnfsTer?
NR_149143.1:n.385dup
NR_149144.1:n.385dup
NM_001354997.3:c.93dup NP_001341926.1:p.Asn32GlnfsTer?
NM_001354998.2:c.93dup NP_001341927.1:p.Asn32GlnfsTer?
NM_018656.5:c.93dup MANE Select NP_061126.2:p.Asn32GlnfsTer?
NR_149143.3:n.295dup
NR_149144.3:n.295dup