Canonical Allele Identifier: CA1509989511

Gene: KLHL2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.165226609_165226611delinsAAC , CM000666.2:g.165226609_165226611delinsAAC	GRCh38
NC_000004.11:g.166147761_166147763delinsAAC , CM000666.1:g.166147761_166147763delinsAAC	GRCh37
NC_000004.10:g.166367211_166367213delinsAAC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000226725.11:c.153-2198_153-2196delinsAAC MANE Select	ENSP00000226725.6:n.153-2198_153-2196delinsAAC
ENST00000226725.10:c.153-2198_153-2196delinsAAC	ENSP00000226725.6:n.153-2198_153-2196delinsAAC
ENST00000421009.6:c.-17-2198_-17-2196delinsAAC	ENSP00000408974.2:n.-17-2198_-17-2196delinsAAC
ENST00000506824.5:c.164+6550_164+6552delinsAAC	ENSP00000421844.1:n.164+6550_164+6552delinsAAC
ENST00000509704.5:c.39-2198_39-2196delinsAAC	ENSP00000421324.1:n.39-2198_39-2196delinsAAC
ENST00000511305.5:c.273-2198_273-2196delinsAAC	ENSP00000422113.1:n.273-2198_273-2196delinsAAC
ENST00000514860.5:c.165-2198_165-2196delinsAAC	ENSP00000424198.1:n.165-2198_165-2196delinsAAC
ENST00000538127.5:c.-6+6550_-6+6552delinsAAC	ENSP00000437526.1:n.-6+6550_-6+6552delinsAAC
NM_001161521.1:c.165-2198_165-2196delinsAAC	NP_001154993.1:n.165-2198_165-2196delinsAAC
NM_001161522.1:c.-6+6550_-6+6552delinsAAC	NP_001154994.1:n.-6+6550_-6+6552delinsAAC
NM_007246.3:c.153-2198_153-2196delinsAAC	NP_009177.3:n.153-2198_153-2196delinsAAC
XM_005262710.2:c.-6+6550_-6+6552delinsAAC	XP_005262767.1:n.-6+6550_-6+6552delinsAAC
XM_011531572.1:c.273-2198_273-2196delinsAAC	XP_011529874.1:n.273-2198_273-2196delinsAAC
XM_011531573.1:c.273-2198_273-2196delinsAAC	XP_011529875.1:n.273-2198_273-2196delinsAAC
XM_011531574.1:c.-17-2198_-17-2196delinsAAC	XP_011529876.1:n.-17-2198_-17-2196delinsAAC
XM_011531575.1:c.-17-2198_-17-2196delinsAAC	XP_011529877.1:n.-17-2198_-17-2196delinsAAC
XM_011531576.1:c.-17-2198_-17-2196delinsAAC	XP_011529878.1:n.-17-2198_-17-2196delinsAAC
XM_011531577.1:c.-118+6550_-118+6552delinsAAC	XP_011529879.1:n.-118+6550_-118+6552delinsAAC
XR_938681.1:n.369-2198_369-2196delinsAAC
XR_938682.1:n.369-2198_369-2196delinsAAC
NM_001331023.1:c.-118+6550_-118+6552delinsAAC	NP_001317952.1:n.-118+6550_-118+6552delinsAAC
NM_001331024.1:c.-17-2198_-17-2196delinsAAC	NP_001317953.1:n.-17-2198_-17-2196delinsAAC
XM_011531572.2:c.273-2198_273-2196delinsAAC	XP_011529874.1:n.273-2198_273-2196delinsAAC
XM_011531576.3:c.-17-2198_-17-2196delinsAAC	XP_011529878.1:n.-17-2198_-17-2196delinsAAC
XM_017007674.1:c.39-2198_39-2196delinsAAC	XP_016863163.1:n.39-2198_39-2196delinsAAC
XM_017007675.2:c.39-2198_39-2196delinsAAC	XP_016863164.1:n.39-2198_39-2196delinsAAC
XM_017007676.1:c.-6+6550_-6+6552delinsAAC	XP_016863165.1:n.-6+6550_-6+6552delinsAAC
XM_024453881.1:c.39-2198_39-2196delinsAAC	XP_024309649.1:n.39-2198_39-2196delinsAAC
XR_001741101.2:n.445-2198_445-2196delinsAAC
XR_001741102.1:n.260-2198_260-2196delinsAAC
XR_002959703.1:n.318-2198_318-2196delinsAAC
XR_002959704.1:n.318-2198_318-2196delinsAAC
XR_002959705.1:n.318-2198_318-2196delinsAAC
NM_007246.4:c.153-2198_153-2196delinsAAC MANE Select	NP_009177.3:n.153-2198_153-2196delinsAAC
NM_001331023.2:c.-118+6550_-118+6552delinsAAC	NP_001317952.1:n.-118+6550_-118+6552delinsAAC
NM_001331024.2:c.-17-2198_-17-2196delinsAAC	NP_001317953.1:n.-17-2198_-17-2196delinsAAC