Canonical Allele Identifier: CA2030832218

Gene: SLC2A13

Linked Data

• dbSNP Id: rs1946386550

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.39960333del , CM000674.2:g.39960333del	GRCh38
NC_000012.11:g.40354135del , CM000674.1:g.40354135del	GRCh37
NC_000012.10:g.38640402del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000280871.9:c.926-8968del MANE Select	ENSP00000280871.4:n.926-8968del
ENST00000280871.8:c.926-8968del	ENSP00000280871.4:n.926-8968del
ENST00000380858.1:c.926-8968del	ENSP00000370239.1:n.926-8968del
NM_052885.3:c.926-8968del	NP_443117.3:n.926-8968del
XM_011537847.1:c.926-8968del	XP_011536149.1:n.926-8968del
XM_011537848.1:c.926-8968del	XP_011536150.1:n.926-8968del
XM_011537849.1:c.926-8968del	XP_011536151.1:n.926-8968del
XM_011537850.1:c.926-8968del	XP_011536152.1:n.926-8968del
XM_011537847.2:c.926-8968del	XP_011536149.1:n.926-8968del
XM_011537849.2:c.926-8968del	XP_011536151.1:n.926-8968del
XM_011537850.3:c.926-8968del	XP_011536152.1:n.926-8968del
XM_017018764.1:c.359-8968del	XP_016874253.1:n.359-8968del
XM_017018765.1:c.359-8968del	XP_016874254.1:n.359-8968del
XM_017018766.1:c.206-8968del	XP_016874255.1:n.206-8968del
XR_001748567.2:n.1203-8968del
XR_001748568.1:n.1203-8968del
NM_052885.4:c.926-8968del MANE Select	NP_443117.3:n.926-8968del