Canonical Allele Identifier: CA2675416137

Gene: KLHL3

Linked Data

• gnomAD v4: 5-137628082-C-CCTCTGCAT

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.137628085_137628092dup , CM000667.2:g.137628085_137628092dup	GRCh38
NC_000005.9:g.136963774_136963781dup , CM000667.1:g.136963774_136963781dup	GRCh37
NC_000005.8:g.136991673_136991680dup	NCBI36
NG_032569.1:g.113001_113008dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309755.9:c.1591+207_1591+214dup MANE Select	ENSP00000312397.4:n.1591+207_1591+214dup
ENST00000309755.8:c.1591+207_1591+214dup	ENSP00000312397.4:n.1591+207_1591+214dup
ENST00000447439.6:n.1647+207_1647+214dup
ENST00000504208.5:c.*475+207_*475+214dup	ENSP00000423585.1:n.*475+207_*475+214dup
ENST00000506491.5:c.1345+207_1345+214dup	ENSP00000424828.1:n.1345+207_1345+214dup
ENST00000506873.5:n.1114+207_1114+214dup
ENST00000508657.5:c.1495+207_1495+214dup	ENSP00000422099.1:n.1495+207_1495+214dup
ENST00000509694.1:n.591_598dup
NM_001257194.1:c.1495+207_1495+214dup	NP_001244123.1:n.1495+207_1495+214dup
NM_001257195.1:c.1345+207_1345+214dup	NP_001244124.1:n.1345+207_1345+214dup
NM_017415.2:c.1591+207_1591+214dup	NP_059111.2:n.1591+207_1591+214dup
NM_017415.3:c.1591+207_1591+214dup MANE Select	NP_059111.2:n.1591+207_1591+214dup
NM_001257195.2:c.1345+207_1345+214dup	NP_001244124.1:n.1345+207_1345+214dup