Canonical Allele Identifier: CA385700287

Gene: SLC35E3

Linked Data

• dbSNP Id: rs1878565082
• MyVariant Identifiers: chr12:g.69140243T>A (hg19) ; chr12:g.68746463T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.68746463T>A , CM000674.2:g.68746463T>A	GRCh38
NC_000012.11:g.69140243T>A , CM000674.1:g.69140243T>A	GRCh37
NC_000012.10:g.67426510T>A	NCBI36
NG_046600.2:g.64513T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000319429.7:n.329T>A
ENST00000398004.4:c.86T>A MANE Select	ENSP00000381089.2:p.Val29Glu
ENST00000673712.1:c.86T>A	ENSP00000501065.1:p.Val29Glu
ENST00000674096.1:c.86T>A	ENSP00000501130.1:p.Val29Glu
ENST00000398004.3:c.86T>A	ENSP00000381089.2:p.Val29Glu
NM_018656.2:c.86T>A	NP_061126.2:p.Val29Glu
XM_005269006.2:c.86T>A	XP_005269063.1:p.Val29Glu
NM_001354997.1:c.86T>A	NP_001341926.1:p.Val29Glu
NM_001354998.1:c.86T>A	NP_001341927.1:p.Val29Glu
NM_018656.3:c.86T>A	NP_061126.2:p.Val29Glu
NR_149143.1:n.378T>A
NR_149144.1:n.378T>A
NM_001354997.3:c.86T>A	NP_001341926.1:p.Val29Glu
NM_001354998.2:c.86T>A	NP_001341927.1:p.Val29Glu
NM_018656.5:c.86T>A MANE Select	NP_061126.2:p.Val29Glu
NR_149143.3:n.288T>A
NR_149144.3:n.288T>A