Canonical Allele Identifier: CA2617441430

Gene: SLC2A14

Linked Data

• gnomAD v4: 12-7818088-T-TC

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.7818089dup , CM000674.2:g.7818089dup	GRCh38
NC_000012.11:g.7970685dup , CM000674.1:g.7970685dup	GRCh37
NC_000012.10:g.7861952dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000431042.7:c.1072-55dup MANE Select	ENSP00000407287.2:n.1072-55dup
ENST00000340749.9:c.1072-55dup	ENSP00000340450.5:n.1072-55dup
ENST00000396589.6:c.1141-55dup	ENSP00000379834.2:n.1141-55dup
ENST00000431042.6:c.1072-55dup	ENSP00000407287.2:n.1072-55dup
ENST00000535295.5:c.814-55dup	ENSP00000440492.1:n.814-55dup
ENST00000539924.5:c.1186-55dup	ENSP00000445929.1:n.1186-55dup
ENST00000542505.5:c.64-55dup	ENSP00000438484.1:n.64-55dup
ENST00000542546.5:c.814-55dup	ENSP00000443903.1:n.814-55dup
ENST00000543909.5:c.1141-55dup	ENSP00000440480.1:n.1141-55dup
ENST00000616981.4:c.1141-55dup	ENSP00000482927.1:n.1141-55dup
NM_001286233.1:c.1141-55dup	NP_001273162.1:n.1141-55dup
NM_001286234.1:c.1072-55dup	NP_001273163.1:n.1072-55dup
NM_001286235.1:c.1072-55dup	NP_001273164.1:n.1072-55dup
NM_001286236.1:c.814-55dup	NP_001273165.1:n.814-55dup
NM_001286237.1:c.1186-55dup	NP_001273166.1:n.1186-55dup
NM_153449.3:c.1141-55dup	NP_703150.1:n.1141-55dup
XM_005253315.2:c.1072-55dup	XP_005253372.1:n.1072-55dup
XM_005253317.3:c.1072-55dup	XP_005253374.1:n.1072-55dup
XM_011520561.1:c.1075-55dup	XP_011518863.1:n.1075-55dup
XM_011520562.1:c.1072-55dup	XP_011518864.1:n.1072-55dup
XM_011520563.1:c.1072-55dup	XP_011518865.1:n.1072-55dup
XM_011520564.1:c.814-55dup	XP_011518866.1:n.814-55dup
XM_011520565.1:c.814-55dup	XP_011518867.1:n.814-55dup
XM_005253315.4:c.1072-55dup	XP_005253372.1:n.1072-55dup
XM_005253317.5:c.1072-55dup	XP_005253374.1:n.1072-55dup
XM_011520563.2:c.1072-55dup	XP_011518865.1:n.1072-55dup
XM_011520564.2:c.814-55dup	XP_011518866.1:n.814-55dup
XM_011520565.2:c.814-55dup	XP_011518867.1:n.814-55dup
XM_017018841.1:c.1144-55dup	XP_016874330.1:n.1144-55dup
XM_017018844.1:c.1144-55dup	XP_016874333.1:n.1144-55dup
XM_017018845.2:c.1144-55dup	XP_016874334.1:n.1144-55dup
XM_017018846.1:c.1072-55dup	XP_016874335.1:n.1072-55dup
XM_017018847.1:c.1072-55dup	XP_016874336.1:n.1072-55dup
XM_024448848.1:c.1144-55dup	XP_024304616.1:n.1144-55dup
XM_024448849.1:c.1072-55dup	XP_024304617.1:n.1072-55dup
NM_001286233.2:c.1141-55dup	NP_001273162.1:n.1141-55dup
NM_001286234.2:c.1072-55dup MANE Select	NP_001273163.1:n.1072-55dup
NM_001286235.2:c.1072-55dup	NP_001273164.1:n.1072-55dup
NM_001286236.2:c.814-55dup	NP_001273165.1:n.814-55dup
NM_001286237.2:c.1186-55dup	NP_001273166.1:n.1186-55dup
NM_153449.4:c.1141-55dup	NP_703150.1:n.1141-55dup