Canonical Allele Identifier: CA361048577

Gene: KLHL3

Linked Data

• MyVariant Identifiers: chr5:g.136975547A>T (hg19) ; chr5:g.137639858A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.137639858A>T , CM000667.2:g.137639858A>T	GRCh38
NC_000005.9:g.136975547A>T , CM000667.1:g.136975547A>T	GRCh37
NC_000005.8:g.137003446A>T	NCBI36
NG_032569.1:g.101233T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000309755.9:c.1021+2T>A MANE Select	ENSP00000312397.4:n.1021+2T>A
ENST00000309755.8:c.1021+2T>A	ENSP00000312397.4:n.1021+2T>A
ENST00000502381.1:n.608+2T>A
ENST00000504208.5:c.*335-11421T>A	ENSP00000423585.1:n.*335-11421T>A
ENST00000505853.1:c.901+2T>A	ENSP00000426173.1:n.901+2T>A
ENST00000506491.5:c.775+2T>A	ENSP00000424828.1:n.775+2T>A
ENST00000506873.5:n.646+2T>A
ENST00000508657.5:c.925+2T>A	ENSP00000422099.1:n.925+2T>A
NM_001257194.1:c.925+2T>A	NP_001244123.1:n.925+2T>A
NM_001257195.1:c.775+2T>A	NP_001244124.1:n.775+2T>A
NM_017415.2:c.1021+2T>A	NP_059111.2:n.1021+2T>A
NM_017415.3:c.1021+2T>A MANE Select	NP_059111.2:n.1021+2T>A
NM_001257195.2:c.775+2T>A	NP_001244124.1:n.775+2T>A