Canonical Allele Identifier: CA2030864987

Gene: SLC2A13

Linked Data

• dbSNP Id: rs1592022776

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40031169C>G , CM000674.2:g.40031169C>G	GRCh38
NC_000012.11:g.40424971C>G , CM000674.1:g.40424971C>G	GRCh37
NC_000012.10:g.38711238C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000280871.9:c.717-2660G>C MANE Select	ENSP00000280871.4:n.717-2660G>C
ENST00000280871.8:c.717-2660G>C	ENSP00000280871.4:n.717-2660G>C
ENST00000380858.1:c.717-2660G>C	ENSP00000370239.1:n.717-2660G>C
NM_052885.3:c.717-2660G>C	NP_443117.3:n.717-2660G>C
XM_011537847.1:c.717-2660G>C	XP_011536149.1:n.717-2660G>C
XM_011537848.1:c.717-2660G>C	XP_011536150.1:n.717-2660G>C
XM_011537849.1:c.717-2660G>C	XP_011536151.1:n.717-2660G>C
XM_011537850.1:c.717-2660G>C	XP_011536152.1:n.717-2660G>C
XM_011537847.2:c.717-2660G>C	XP_011536149.1:n.717-2660G>C
XM_011537849.2:c.717-2660G>C	XP_011536151.1:n.717-2660G>C
XM_011537850.3:c.717-2660G>C	XP_011536152.1:n.717-2660G>C
XM_017018764.1:c.150-2660G>C	XP_016874253.1:n.150-2660G>C
XM_017018765.1:c.150-2660G>C	XP_016874254.1:n.150-2660G>C
XR_001748567.2:n.994-2660G>C
XR_001748568.1:n.994-2660G>C
NM_052885.4:c.717-2660G>C MANE Select	NP_443117.3:n.717-2660G>C