Canonical Allele Identifier: CA2675417791

Gene: KLHL3

Linked Data

• gnomAD v4: 5-137639774-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.137639774A>G , CM000667.2:g.137639774A>G	GRCh38
NC_000005.9:g.136975463A>G , CM000667.1:g.136975463A>G	GRCh37
NC_000005.8:g.137003362A>G	NCBI36
NG_032569.1:g.101317T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000309755.9:c.1021+86T>C MANE Select	ENSP00000312397.4:n.1021+86T>C
ENST00000309755.8:c.1021+86T>C	ENSP00000312397.4:n.1021+86T>C
ENST00000502381.1:n.608+86T>C
ENST00000504208.5:c.*335-11337T>C	ENSP00000423585.1:n.*335-11337T>C
ENST00000505853.1:c.901+86T>C	ENSP00000426173.1:n.901+86T>C
ENST00000506491.5:c.775+86T>C	ENSP00000424828.1:n.775+86T>C
ENST00000506873.5:n.646+86T>C
ENST00000508657.5:c.925+86T>C	ENSP00000422099.1:n.925+86T>C
NM_001257194.1:c.925+86T>C	NP_001244123.1:n.925+86T>C
NM_001257195.1:c.775+86T>C	NP_001244124.1:n.775+86T>C
NM_017415.2:c.1021+86T>C	NP_059111.2:n.1021+86T>C
NM_017415.3:c.1021+86T>C MANE Select	NP_059111.2:n.1021+86T>C
NM_001257195.2:c.775+86T>C	NP_001244124.1:n.775+86T>C