Canonical Allele Identifier: CA385700529
Gene: SLC35E3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.68746574T>G , CM000674.2:g.68746574T>G GRCh38
NC_000012.11:g.69140354T>G , CM000674.1:g.69140354T>G GRCh37
NC_000012.10:g.67426621T>G NCBI36
NG_046600.2:g.64624T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000319429.7:n.440T>G
ENST00000398004.4:c.197T>G MANE Select ENSP00000381089.2:p.Ile66Ser
ENST00000673712.1:c.197T>G ENSP00000501065.1:p.Ile66Ser
ENST00000674096.1:c.197T>G ENSP00000501130.1:p.Ile66Ser
ENST00000398004.3:c.197T>G ENSP00000381089.2:p.Ile66Ser
NM_018656.2:c.197T>G NP_061126.2:p.Ile66Ser
XM_005269006.2:c.197T>G XP_005269063.1:p.Ile66Ser
NM_001354997.1:c.197T>G NP_001341926.1:p.Ile66Ser
NM_001354998.1:c.197T>G NP_001341927.1:p.Ile66Ser
NM_018656.3:c.197T>G NP_061126.2:p.Ile66Ser
NR_149143.1:n.489T>G
NR_149144.1:n.489T>G
NM_001354997.3:c.197T>G NP_001341926.1:p.Ile66Ser
NM_001354998.2:c.197T>G NP_001341927.1:p.Ile66Ser
NM_018656.5:c.197T>G MANE Select NP_061126.2:p.Ile66Ser
NR_149143.3:n.399T>G
NR_149144.3:n.399T>G