Canonical Allele Identifier: CA361048051

Gene: KLHL3

Linked Data

• COSMIC: COSM5765453
• MyVariant Identifiers: chr5:g.136974731A>G (hg19) ; chr5:g.137639042A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.137639042A>G , CM000667.2:g.137639042A>G	GRCh38
NC_000005.9:g.136974731A>G , CM000667.1:g.136974731A>G	GRCh37
NC_000005.8:g.137002630A>G	NCBI36
NG_032569.1:g.102049T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309755.9:c.1130T>C MANE Select	ENSP00000312397.4:p.Ile377Thr
ENST00000309755.8:c.1130T>C	ENSP00000312397.4:p.Ile377Thr
ENST00000502381.1:n.717T>C
ENST00000504208.5:c.*335-10605T>C	ENSP00000423585.1:n.*335-10605T>C
ENST00000505853.1:c.1010T>C	ENSP00000426173.1:p.Ile337Thr
ENST00000506491.5:c.884T>C	ENSP00000424828.1:p.Ile295Thr
ENST00000506873.5:n.755T>C
ENST00000508657.5:c.1034T>C	ENSP00000422099.1:p.Ile345Thr
NM_001257194.1:c.1034T>C	NP_001244123.1:p.Ile345Thr
NM_001257195.1:c.884T>C	NP_001244124.1:p.Ile295Thr
NM_017415.2:c.1130T>C	NP_059111.2:p.Ile377Thr
NM_017415.3:c.1130T>C MANE Select	NP_059111.2:p.Ile377Thr
NM_001257195.2:c.884T>C	NP_001244124.1:p.Ile295Thr