Canonical Allele Identifier: CA1585511337

Gene: KLHL3

Linked Data

• dbSNP Id: rs1750527470

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.137628136_137628145dup , CM000667.2:g.137628136_137628145dup	GRCh38
NC_000005.9:g.136963825_136963834dup , CM000667.1:g.136963825_136963834dup	GRCh37
NC_000005.8:g.136991724_136991733dup	NCBI36
NG_032569.1:g.112946_112955dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309755.9:c.1591+152_1591+161dup MANE Select	ENSP00000312397.4:n.1591+152_1591+161dup
ENST00000309755.8:c.1591+152_1591+161dup	ENSP00000312397.4:n.1591+152_1591+161dup
ENST00000447439.6:n.1647+152_1647+161dup
ENST00000504208.5:c.*475+152_*475+161dup	ENSP00000423585.1:n.*475+152_*475+161dup
ENST00000506491.5:c.1345+152_1345+161dup	ENSP00000424828.1:n.1345+152_1345+161dup
ENST00000506873.5:n.1114+152_1114+161dup
ENST00000508657.5:c.1495+152_1495+161dup	ENSP00000422099.1:n.1495+152_1495+161dup
ENST00000509694.1:n.536_545dup
NM_001257194.1:c.1495+152_1495+161dup	NP_001244123.1:n.1495+152_1495+161dup
NM_001257195.1:c.1345+152_1345+161dup	NP_001244124.1:n.1345+152_1345+161dup
NM_017415.2:c.1591+152_1591+161dup	NP_059111.2:n.1591+152_1591+161dup
NM_017415.3:c.1591+152_1591+161dup MANE Select	NP_059111.2:n.1591+152_1591+161dup
NM_001257195.2:c.1345+152_1345+161dup	NP_001244124.1:n.1345+152_1345+161dup