Canonical Allele Identifier: CA13619275
Gene: SLC2A13 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs11174478

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.39960442G>A , CM000674.2:g.39960442G>A GRCh38
NC_000012.11:g.40354244G>A , CM000674.1:g.40354244G>A GRCh37
NC_000012.10:g.38640511G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_052885.3:c.926-9077C>T VV NP_443117.3:p.=
XM_011537847.1:c.926-9077C>T XP_011536149.1:p.=
XM_011537848.1:c.926-9077C>T XP_011536150.1:p.=
XM_011537849.1:c.926-9077C>T XP_011536151.1:p.=
XM_011537850.1:c.926-9077C>T XP_011536152.1:p.=
XM_011537847.2:c.926-9077C>T XP_011536149.1:p.=
XM_011537849.2:c.926-9077C>T XP_011536151.1:p.=
XM_011537850.3:c.926-9077C>T XP_011536152.1:p.=
XM_017018764.1:c.359-9077C>T XP_016874253.1:p.=
XM_017018765.1:c.359-9077C>T XP_016874254.1:p.=
XM_017018766.1:c.206-9077C>T XP_016874255.1:p.=
XR_001748567.2:n.1203-9077C>T
XR_001748568.1:n.1203-9077C>T
NM_052885.4:c.926-9077C>T VV MANE Preferred NP_443117.3:p.=
ENST00000280871.8:c.926-9077C>T ENSP00000280871.4:p.=
ENST00000380858.1:c.926-9077C>T ENSP00000370239.1:p.=