Canonical Allele Identifier: CA2030832242

Gene: SLC2A13

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.39960345G= , CM000674.2:g.39960345G=	GRCh38
NC_000012.11:g.40354147G= , CM000674.1:g.40354147G=	GRCh37
NC_000012.10:g.38640414G=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000280871.9:c.926-8980C= MANE Select	ENSP00000280871.4:n.926-8980C=
ENST00000280871.8:c.926-8980C=	ENSP00000280871.4:n.926-8980C=
ENST00000380858.1:c.926-8980C=	ENSP00000370239.1:n.926-8980C=
NM_052885.3:c.926-8980C=	NP_443117.3:n.926-8980C=
XM_011537847.1:c.926-8980C=	XP_011536149.1:n.926-8980C=
XM_011537848.1:c.926-8980C=	XP_011536150.1:n.926-8980C=
XM_011537849.1:c.926-8980C=	XP_011536151.1:n.926-8980C=
XM_011537850.1:c.926-8980C=	XP_011536152.1:n.926-8980C=
XM_011537847.2:c.926-8980C=	XP_011536149.1:n.926-8980C=
XM_011537849.2:c.926-8980C=	XP_011536151.1:n.926-8980C=
XM_011537850.3:c.926-8980C=	XP_011536152.1:n.926-8980C=
XM_017018764.1:c.359-8980C=	XP_016874253.1:n.359-8980C=
XM_017018765.1:c.359-8980C=	XP_016874254.1:n.359-8980C=
XM_017018766.1:c.206-8980C=	XP_016874255.1:n.206-8980C=
XR_001748567.2:n.1203-8980C=
XR_001748568.1:n.1203-8980C=
NM_052885.4:c.926-8980C= MANE Select	NP_443117.3:n.926-8980C=