Canonical Allele Identifier: CA385700491
Gene: SLC35E3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.69140338T>A (hg19) chr12:g.68746558T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.68746558T>A , CM000674.2:g.68746558T>A GRCh38
NC_000012.11:g.69140338T>A , CM000674.1:g.69140338T>A GRCh37
NC_000012.10:g.67426605T>A NCBI36
NG_046600.2:g.64608T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000319429.7:n.424T>A
ENST00000398004.4:c.181T>A MANE Select ENSP00000381089.2:p.Cys61Ser
ENST00000673712.1:c.181T>A ENSP00000501065.1:p.Cys61Ser
ENST00000674096.1:c.181T>A ENSP00000501130.1:p.Cys61Ser
ENST00000398004.3:c.181T>A ENSP00000381089.2:p.Cys61Ser
NM_018656.2:c.181T>A NP_061126.2:p.Cys61Ser
XM_005269006.2:c.181T>A XP_005269063.1:p.Cys61Ser
NM_001354997.1:c.181T>A NP_001341926.1:p.Cys61Ser
NM_001354998.1:c.181T>A NP_001341927.1:p.Cys61Ser
NM_018656.3:c.181T>A NP_061126.2:p.Cys61Ser
NR_149143.1:n.473T>A
NR_149144.1:n.473T>A
NM_001354997.3:c.181T>A NP_001341926.1:p.Cys61Ser
NM_001354998.2:c.181T>A NP_001341927.1:p.Cys61Ser
NM_018656.5:c.181T>A MANE Select NP_061126.2:p.Cys61Ser
NR_149143.3:n.383T>A
NR_149144.3:n.383T>A
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