Canonical Allele Identifier: CA1081988664

Gene: KLHL3

Linked Data

• gnomAD v3: 5-137639700-ACG-A
• gnomAD v4: 5-137639700-ACG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.137639701_137639702del , CM000667.2:g.137639701_137639702del	GRCh38
NC_000005.9:g.136975390_136975391del , CM000667.1:g.136975390_136975391del	GRCh37
NC_000005.8:g.137003289_137003290del	NCBI36
NG_032569.1:g.101389_101390del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309755.9:c.1021+158_1021+159del MANE Select	ENSP00000312397.4:n.1021+158_1021+159del
ENST00000309755.8:c.1021+158_1021+159del	ENSP00000312397.4:n.1021+158_1021+159del
ENST00000502381.1:n.608+158_608+159del
ENST00000504208.5:c.*335-11265_*335-11264del	ENSP00000423585.1:n.*335-11265_*335-11264del
ENST00000505853.1:c.901+158_901+159del	ENSP00000426173.1:n.901+158_901+159del
ENST00000506491.5:c.775+158_775+159del	ENSP00000424828.1:n.775+158_775+159del
ENST00000506873.5:n.646+158_646+159del
ENST00000508657.5:c.925+158_925+159del	ENSP00000422099.1:n.925+158_925+159del
NM_001257194.1:c.925+158_925+159del	NP_001244123.1:n.925+158_925+159del
NM_001257195.1:c.775+158_775+159del	NP_001244124.1:n.775+158_775+159del
NM_017415.2:c.1021+158_1021+159del	NP_059111.2:n.1021+158_1021+159del
NM_017415.3:c.1021+158_1021+159del MANE Select	NP_059111.2:n.1021+158_1021+159del
NM_001257195.2:c.775+158_775+159del	NP_001244124.1:n.775+158_775+159del