Canonical Allele Identifier: CA2830535197

Gene: KLHL2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.165305918_165305919insACAC , CM000666.2:g.165305918_165305919insACAC	GRCh38
NC_000004.11:g.166227070_166227071insACAC , CM000666.1:g.166227070_166227071insACAC	GRCh37
NC_000004.10:g.166446520_166446521insACAC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000226725.11:c.1039+193_1039+194insACAC MANE Select	ENSP00000226725.6:n.1039+193_1039+194insACAC
ENST00000226725.10:c.1039+193_1039+194insACAC	ENSP00000226725.6:n.1039+193_1039+194insACAC
ENST00000421009.6:c.748+193_748+194insACAC	ENSP00000408974.2:n.748+193_748+194insACAC
ENST00000506541.5:n.619+193_619+194insACAC
ENST00000506761.1:c.541+193_541+194insACAC	ENSP00000424108.1:n.541+193_541+194insACAC
ENST00000506824.5:c.*776+193_*776+194insACAC	ENSP00000421844.1:n.*776+193_*776+194insACAC
ENST00000509028.1:n.481-4635_481-4634insACAC
ENST00000514860.5:c.1051+193_1051+194insACAC	ENSP00000424198.1:n.1051+193_1051+194insACAC
ENST00000538127.5:c.775+193_775+194insACAC	ENSP00000437526.1:n.775+193_775+194insACAC
NM_001161521.1:c.1051+193_1051+194insACAC	NP_001154993.1:n.1051+193_1051+194insACAC
NM_001161522.1:c.775+193_775+194insACAC	NP_001154994.1:n.775+193_775+194insACAC
NM_007246.3:c.1039+193_1039+194insACAC	NP_009177.3:n.1039+193_1039+194insACAC
XM_005262710.2:c.775+193_775+194insACAC	XP_005262767.1:n.775+193_775+194insACAC
XM_011531572.1:c.1159+193_1159+194insACAC	XP_011529874.1:n.1159+193_1159+194insACAC
XM_011531573.1:c.1159+193_1159+194insACAC	XP_011529875.1:n.1159+193_1159+194insACAC
XM_011531574.1:c.748+193_748+194insACAC	XP_011529876.1:n.748+193_748+194insACAC
XM_011531575.1:c.748+193_748+194insACAC	XP_011529877.1:n.748+193_748+194insACAC
XM_011531576.1:c.748+193_748+194insACAC	XP_011529878.1:n.748+193_748+194insACAC
XM_011531577.1:c.541+193_541+194insACAC	XP_011529879.1:n.541+193_541+194insACAC
XR_938681.1:n.1255+193_1255+194insACAC
XR_938682.1:n.1138-4635_1138-4634insACAC
NM_001331023.1:c.541+193_541+194insACAC	NP_001317952.1:n.541+193_541+194insACAC
NM_001331024.1:c.748+193_748+194insACAC	NP_001317953.1:n.748+193_748+194insACAC
XM_011531572.2:c.1159+193_1159+194insACAC	XP_011529874.1:n.1159+193_1159+194insACAC
XM_011531576.3:c.748+193_748+194insACAC	XP_011529878.1:n.748+193_748+194insACAC
XM_017007674.1:c.925+193_925+194insACAC	XP_016863163.1:n.925+193_925+194insACAC
XM_017007675.2:c.925+193_925+194insACAC	XP_016863164.1:n.925+193_925+194insACAC
XM_017007676.1:c.775+193_775+194insACAC	XP_016863165.1:n.775+193_775+194insACAC
XM_024453881.1:c.925+193_925+194insACAC	XP_024309649.1:n.925+193_925+194insACAC
XR_001741101.2:n.1331+193_1331+194insACAC
XR_001741102.1:n.1146+193_1146+194insACAC
XR_002959703.1:n.1204+193_1204+194insACAC
XR_002959704.1:n.1087-4635_1087-4634insACAC
XR_002959705.1:n.1087-4635_1087-4634insACAC
NM_007246.4:c.1039+193_1039+194insACAC MANE Select	NP_009177.3:n.1039+193_1039+194insACAC
NM_001331023.2:c.541+193_541+194insACAC	NP_001317952.1:n.541+193_541+194insACAC
NM_001331024.2:c.748+193_748+194insACAC	NP_001317953.1:n.748+193_748+194insACAC