Canonical Allele Identifier: CA2030868939

Gene: SLC2A13

Linked Data

• dbSNP Id: rs1947951979

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40034733_40034734del , CM000674.2:g.40034733_40034734del	GRCh38
NC_000012.11:g.40428535_40428536del , CM000674.1:g.40428535_40428536del	GRCh37
NC_000012.10:g.38714802_38714803del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000280871.9:c.717-6223_717-6222del MANE Select	ENSP00000280871.4:n.717-6223_717-6222del
ENST00000280871.8:c.717-6223_717-6222del	ENSP00000280871.4:n.717-6223_717-6222del
ENST00000380858.1:c.717-6223_717-6222del	ENSP00000370239.1:n.717-6223_717-6222del
NM_052885.3:c.717-6223_717-6222del	NP_443117.3:n.717-6223_717-6222del
XM_011537847.1:c.717-6223_717-6222del	XP_011536149.1:n.717-6223_717-6222del
XM_011537848.1:c.717-6223_717-6222del	XP_011536150.1:n.717-6223_717-6222del
XM_011537849.1:c.717-6223_717-6222del	XP_011536151.1:n.717-6223_717-6222del
XM_011537850.1:c.717-6223_717-6222del	XP_011536152.1:n.717-6223_717-6222del
XM_011537847.2:c.717-6223_717-6222del	XP_011536149.1:n.717-6223_717-6222del
XM_011537849.2:c.717-6223_717-6222del	XP_011536151.1:n.717-6223_717-6222del
XM_011537850.3:c.717-6223_717-6222del	XP_011536152.1:n.717-6223_717-6222del
XM_017018764.1:c.150-6223_150-6222del	XP_016874253.1:n.150-6223_150-6222del
XM_017018765.1:c.150-6223_150-6222del	XP_016874254.1:n.150-6223_150-6222del
XR_001748567.2:n.994-6223_994-6222del
XR_001748568.1:n.994-6223_994-6222del
NM_052885.4:c.717-6223_717-6222del MANE Select	NP_443117.3:n.717-6223_717-6222del