Canonical Allele Identifier: CA361048407

Gene: KLHL3

Linked Data

• MyVariant Identifiers: chr5:g.136974815A>G (hg19) ; chr5:g.137639126A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.137639126A>G , CM000667.2:g.137639126A>G	GRCh38
NC_000005.9:g.136974815A>G , CM000667.1:g.136974815A>G	GRCh37
NC_000005.8:g.137002714A>G	NCBI36
NG_032569.1:g.101965T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309755.9:c.1046T>C MANE Select	ENSP00000312397.4:p.Val349Ala
ENST00000309755.8:c.1046T>C	ENSP00000312397.4:p.Val349Ala
ENST00000502381.1:n.633T>C
ENST00000504208.5:c.*335-10689T>C	ENSP00000423585.1:n.*335-10689T>C
ENST00000505853.1:c.926T>C	ENSP00000426173.1:p.Val309Ala
ENST00000506491.5:c.800T>C	ENSP00000424828.1:p.Val267Ala
ENST00000506873.5:n.671T>C
ENST00000508657.5:c.950T>C	ENSP00000422099.1:p.Val317Ala
NM_001257194.1:c.950T>C	NP_001244123.1:p.Val317Ala
NM_001257195.1:c.800T>C	NP_001244124.1:p.Val267Ala
NM_017415.2:c.1046T>C	NP_059111.2:p.Val349Ala
NM_017415.3:c.1046T>C MANE Select	NP_059111.2:p.Val349Ala
NM_001257195.2:c.800T>C	NP_001244124.1:p.Val267Ala