Canonical Allele Identifier: CA2030832238

Gene: SLC2A13

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.39960343C= , CM000674.2:g.39960343C=	GRCh38
NC_000012.11:g.40354145C= , CM000674.1:g.40354145C=	GRCh37
NC_000012.10:g.38640412C=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000280871.9:c.926-8978G= MANE Select	ENSP00000280871.4:n.926-8978G=
ENST00000280871.8:c.926-8978G=	ENSP00000280871.4:n.926-8978G=
ENST00000380858.1:c.926-8978G=	ENSP00000370239.1:n.926-8978G=
NM_052885.3:c.926-8978G=	NP_443117.3:n.926-8978G=
XM_011537847.1:c.926-8978G=	XP_011536149.1:n.926-8978G=
XM_011537848.1:c.926-8978G=	XP_011536150.1:n.926-8978G=
XM_011537849.1:c.926-8978G=	XP_011536151.1:n.926-8978G=
XM_011537850.1:c.926-8978G=	XP_011536152.1:n.926-8978G=
XM_011537847.2:c.926-8978G=	XP_011536149.1:n.926-8978G=
XM_011537849.2:c.926-8978G=	XP_011536151.1:n.926-8978G=
XM_011537850.3:c.926-8978G=	XP_011536152.1:n.926-8978G=
XM_017018764.1:c.359-8978G=	XP_016874253.1:n.359-8978G=
XM_017018765.1:c.359-8978G=	XP_016874254.1:n.359-8978G=
XM_017018766.1:c.206-8978G=	XP_016874255.1:n.206-8978G=
XR_001748567.2:n.1203-8978G=
XR_001748568.1:n.1203-8978G=
NM_052885.4:c.926-8978G= MANE Select	NP_443117.3:n.926-8978G=