Canonical Allele Identifier: CA691332298

Gene: SLC35E3

Linked Data

• dbSNP Id: rs1268904726
• MyVariant Identifiers: chr12:g.69140320_69140321insG (hg19) ; chr12:g.68746540_68746541insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.68746542dup , CM000674.2:g.68746542dup	GRCh38
NC_000012.11:g.69140322dup , CM000674.1:g.69140322dup	GRCh37
NC_000012.10:g.67426589dup	NCBI36
NG_046600.2:g.64592dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000319429.7:n.408dup
ENST00000398004.4:c.165dup MANE Select	ENSP00000381089.2:p.Leu56AlafsTer?
ENST00000673712.1:c.165dup	ENSP00000501065.1:p.Leu56AlafsTer?
ENST00000674096.1:c.165dup	ENSP00000501130.1:p.Leu56AlafsTer?
ENST00000398004.3:c.165dup	ENSP00000381089.2:p.Leu56AlafsTer?
NM_018656.2:c.165dup	NP_061126.2:p.Leu56AlafsTer?
XM_005269006.2:c.165dup	XP_005269063.1:p.Leu56AlafsTer?
NM_001354997.1:c.165dup	NP_001341926.1:p.Leu56AlafsTer?
NM_001354998.1:c.165dup	NP_001341927.1:p.Leu56AlafsTer?
NM_018656.3:c.165dup	NP_061126.2:p.Leu56AlafsTer?
NR_149143.1:n.457dup
NR_149144.1:n.457dup
NM_001354997.3:c.165dup	NP_001341926.1:p.Leu56AlafsTer?
NM_001354998.2:c.165dup	NP_001341927.1:p.Leu56AlafsTer?
NM_018656.5:c.165dup MANE Select	NP_061126.2:p.Leu56AlafsTer?
NR_149143.3:n.367dup
NR_149144.3:n.367dup