Canonical Allele Identifier: CA688726030

Gene: SLC2A13 REDIC1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.39775543dup , CM000674.2:g.39775543dup	GRCh38
NC_000012.11:g.40169345dup , CM000674.1:g.40169345dup	GRCh37
NC_000012.10:g.38455612dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_052885.4:c.1446-10685dup (SLC2A13) MANE Select	NP_443117.3:n.1446-10685dup
ENST00000280871.9:c.1446-10685dup (SLC2A13) MANE Select	ENSP00000280871.4:n.1446-10685dup
NM_052885.3:c.1446-10685dup (SLC2A13)	NP_443117.3:n.1446-10685dup
NR_135051.1:n.2241+10734dup (REDIC1)
NR_135051.2:n.2225+10734dup (REDIC1)
ENST00000280871.8:c.1446-10685dup (SLC2A13)	ENSP00000280871.4:n.1446-10685dup
ENST00000468200.2:c.*794+10734dup (REDIC1)	ENSP00000473371.1:n.*794+10734dup
XM_011537847.1:c.1320-10685dup (SLC2A13)	XP_011536149.1:n.1320-10685dup
XM_011537847.2:c.1320-10685dup (SLC2A13)	XP_011536149.1:n.1320-10685dup
XM_017018764.1:c.879-10685dup (SLC2A13)	XP_016874253.1:n.879-10685dup
XM_017018765.1:c.879-10685dup (SLC2A13)	XP_016874254.1:n.879-10685dup
XM_017018766.1:c.726-10685dup (SLC2A13)	XP_016874255.1:n.726-10685dup
XR_001748567.2:n.1797-10685dup (SLC2A13)
XR_001748568.1:n.1813-10685dup (SLC2A13)
XR_944862.1:n.117-13045dup