Canonical Allele Identifier: CA385700500
Gene: SLC35E3 HGNC NCBI

Linked Data

dbSNP Id: rs1435525843

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.68746561C>T , CM000674.2:g.68746561C>T GRCh38
NC_000012.11:g.69140341C>T , CM000674.1:g.69140341C>T GRCh37
NC_000012.10:g.67426608C>T NCBI36
NG_046600.2:g.64611C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000319429.7:n.427C>T
ENST00000398004.4:c.184C>T MANE Select ENSP00000381089.2:p.Gln62Ter
ENST00000673712.1:c.184C>T ENSP00000501065.1:p.Gln62Ter
ENST00000674096.1:c.184C>T ENSP00000501130.1:p.Gln62Ter
ENST00000398004.3:c.184C>T ENSP00000381089.2:p.Gln62Ter
NM_018656.2:c.184C>T NP_061126.2:p.Gln62Ter
XM_005269006.2:c.184C>T XP_005269063.1:p.Gln62Ter
NM_001354997.1:c.184C>T NP_001341926.1:p.Gln62Ter
NM_001354998.1:c.184C>T NP_001341927.1:p.Gln62Ter
NM_018656.3:c.184C>T NP_061126.2:p.Gln62Ter
NR_149143.1:n.476C>T
NR_149144.1:n.476C>T
NM_001354997.3:c.184C>T NP_001341926.1:p.Gln62Ter
NM_001354998.2:c.184C>T NP_001341927.1:p.Gln62Ter
NM_018656.5:c.184C>T MANE Select NP_061126.2:p.Gln62Ter
NR_149143.3:n.386C>T
NR_149144.3:n.386C>T