Canonical Allele Identifier: CA2030819474

Gene: SLC2A13

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.39947276_39947277delinsTC , CM000674.2:g.39947276_39947277delinsTC	GRCh38
NC_000012.11:g.40341078_40341079delinsTC , CM000674.1:g.40341078_40341079delinsTC	GRCh37
NC_000012.10:g.38627345_38627346delinsTC	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000280871.9:c.1034+3980_1034+3981delinsGA MANE Select	ENSP00000280871.4:n.1034+3980_1034+3981de...
ENST00000280871.8:c.1034+3980_1034+3981delinsGA	ENSP00000280871.4:n.1034+3980_1034+3981de...
NM_052885.3:c.1034+3980_1034+3981delinsGA	NP_443117.3:n.1034+3980_1034+3981delinsGA...
XM_011537847.1:c.1034+3980_1034+3981delinsGA	XP_011536149.1:n.1034+3980_1034+3981delin...
XM_011537848.1:c.1034+3980_1034+3981delinsGA	XP_011536150.1:n.1034+3980_1034+3981delin...
XM_011537849.1:c.1034+3980_1034+3981delinsGA	XP_011536151.1:n.1034+3980_1034+3981delin...
XM_011537850.1:c.1034+3980_1034+3981delinsGA	XP_011536152.1:n.1034+3980_1034+3981delin...
XM_011537847.2:c.1034+3980_1034+3981delinsGA	XP_011536149.1:n.1034+3980_1034+3981delin...
XM_011537849.2:c.1034+3980_1034+3981delinsGA	XP_011536151.1:n.1034+3980_1034+3981delin...
XM_011537850.3:c.1034+3980_1034+3981delinsGA	XP_011536152.1:n.1034+3980_1034+3981delin...
XM_017018764.1:c.467+3980_467+3981delinsGA	XP_016874253.1:n.467+3980_467+3981delinsG...
XM_017018765.1:c.467+3980_467+3981delinsGA	XP_016874254.1:n.467+3980_467+3981delinsG...
XM_017018766.1:c.314+3980_314+3981delinsGA	XP_016874255.1:n.314+3980_314+3981delinsG...
XR_001748567.2:n.1311+3980_1311+3981delinsGA
XR_001748568.1:n.1311+3980_1311+3981delinsGA
NM_052885.4:c.1034+3980_1034+3981delinsGA MANE Select	NP_443117.3:n.1034+3980_1034+3981delinsGA...