Canonical Allele Identifier: CA13586498
Gene: SLC2A13 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs11174812

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.40031285C>T , CM000674.2:g.40031285C>T GRCh38
NC_000012.11:g.40425087C>T , CM000674.1:g.40425087C>T GRCh37
NC_000012.10:g.38711354C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_052885.3:c.717-2776G>A VV NP_443117.3:p.=
XM_011537847.1:c.717-2776G>A XP_011536149.1:p.=
XM_011537848.1:c.717-2776G>A XP_011536150.1:p.=
XM_011537849.1:c.717-2776G>A XP_011536151.1:p.=
XM_011537850.1:c.717-2776G>A XP_011536152.1:p.=
XM_011537847.2:c.717-2776G>A
XM_011537849.2:c.717-2776G>A
XM_011537850.3:c.717-2776G>A
XM_017018764.1:c.150-2776G>A XP_016874253.1:p.=
XM_017018765.1:c.150-2776G>A XP_016874254.1:p.=
XR_001748567.2:n.994-2776G>A
XR_001748568.1:n.994-2776G>A
ENST00000280871.8:c.717-2776G>A ENSP00000280871.4:p.=
ENST00000380858.1:c.717-2776G>A ENSP00000370239.1:p.=