Canonical Allele Identifier: CA2030819293
Gene: SLC2A13 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.39947067_39947085delinsGTCTAACTTGACTCAGCTC , CM000674.2:g.39947067_39947085delinsGTCTAACTTGACTCAGCTC GRCh38
NC_000012.11:g.40340869_40340887delinsGTCTAACTTGACTCAGCTC , CM000674.1:g.40340869_40340887delinsGTCTAACTTGACTCAGCTC GRCh37
NC_000012.10:g.38627136_38627154delinsGTCTAACTTGACTCAGCTC NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000280871.9:c.1034+4172_1034+4190delinsGAGCTGAGTCAAGTTAGAC MANE Select ENSP00000280871.4:n.1034+4172_1034+4190delinsGAGCTGAGTCAAGTTA...
ENST00000280871.8:c.1034+4172_1034+4190delinsGAGCTGAGTCAAGTTAGAC ENSP00000280871.4:n.1034+4172_1034+4190delinsGAGCTGAGTCAAGTTA...
NM_052885.3:c.1034+4172_1034+4190delinsGAGCTGAGTCAAGTTAGAC NP_443117.3:n.1034+4172_1034+4190delinsGAGCTGAGTCAAGTTAGAC
XM_011537847.1:c.1034+4172_1034+4190delinsGAGCTGAGTCAAGTTAGAC XP_011536149.1:n.1034+4172_1034+4190delinsGAGCTGAGTCAAGTTAGAC...
XM_011537848.1:c.1034+4172_1034+4190delinsGAGCTGAGTCAAGTTAGAC XP_011536150.1:n.1034+4172_1034+4190delinsGAGCTGAGTCAAGTTAGAC...
XM_011537849.1:c.1034+4172_1034+4190delinsGAGCTGAGTCAAGTTAGAC XP_011536151.1:n.1034+4172_1034+4190delinsGAGCTGAGTCAAGTTAGAC...
XM_011537850.1:c.1034+4172_1034+4190delinsGAGCTGAGTCAAGTTAGAC XP_011536152.1:n.1034+4172_1034+4190delinsGAGCTGAGTCAAGTTAGAC...
XM_011537847.2:c.1034+4172_1034+4190delinsGAGCTGAGTCAAGTTAGAC XP_011536149.1:n.1034+4172_1034+4190delinsGAGCTGAGTCAAGTTAGAC...
XM_011537849.2:c.1034+4172_1034+4190delinsGAGCTGAGTCAAGTTAGAC XP_011536151.1:n.1034+4172_1034+4190delinsGAGCTGAGTCAAGTTAGAC...
XM_011537850.3:c.1034+4172_1034+4190delinsGAGCTGAGTCAAGTTAGAC XP_011536152.1:n.1034+4172_1034+4190delinsGAGCTGAGTCAAGTTAGAC...
XM_017018764.1:c.467+4172_467+4190delinsGAGCTGAGTCAAGTTAGAC XP_016874253.1:n.467+4172_467+4190delinsGAGCTGAGTCAAGTTAGAC
XM_017018765.1:c.467+4172_467+4190delinsGAGCTGAGTCAAGTTAGAC XP_016874254.1:n.467+4172_467+4190delinsGAGCTGAGTCAAGTTAGAC
XM_017018766.1:c.314+4172_314+4190delinsGAGCTGAGTCAAGTTAGAC XP_016874255.1:n.314+4172_314+4190delinsGAGCTGAGTCAAGTTAGAC
XR_001748567.2:n.1311+4172_1311+4190delinsGAGCTGAGTCAAGTTAGAC
XR_001748568.1:n.1311+4172_1311+4190delinsGAGCTGAGTCAAGTTAGAC
NM_052885.4:c.1034+4172_1034+4190delinsGAGCTGAGTCAAGTTAGAC MANE Select NP_443117.3:n.1034+4172_1034+4190delinsGAGCTGAGTCAAGTTAGAC