Canonical Allele Identifier: CA480520895

Gene: SLC35E3

Linked Data

• MyVariant Identifiers: chr12:g.69140514C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.68746734C>G , CM000674.2:g.68746734C>G	GRCh38
NC_000012.11:g.69140514C>G , CM000674.1:g.69140514C>G	GRCh37
NC_000012.10:g.67426781C>G	NCBI36
NG_046600.2:g.64784C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000319429.7:n.600C>G
ENST00000398004.4:c.357C>G MANE Select	ENSP00000381089.2:p.Thr119=
ENST00000673712.1:c.357C>G	ENSP00000501065.1:p.Thr119=
ENST00000674096.1:c.357C>G	ENSP00000501130.1:p.Thr119=
ENST00000398004.3:c.357C>G	ENSP00000381089.2:p.Thr119=
NM_018656.2:c.357C>G	NP_061126.2:p.Thr119=
XM_005269006.2:c.357C>G	XP_005269063.1:p.Thr119=
NM_001354997.1:c.357C>G	NP_001341926.1:p.Thr119=
NM_001354998.1:c.357C>G	NP_001341927.1:p.Thr119=
NM_018656.3:c.357C>G	NP_061126.2:p.Thr119=
NR_149143.1:n.649C>G
NR_149144.1:n.649C>G
NM_001354997.3:c.357C>G	NP_001341926.1:p.Thr119=
NM_001354998.2:c.357C>G	NP_001341927.1:p.Thr119=
NM_018656.5:c.357C>G MANE Select	NP_061126.2:p.Thr119=
NR_149143.3:n.559C>G
NR_149144.3:n.559C>G