Canonical Allele Identifier: CA361048368

Gene: KLHL3

Linked Data

• MyVariant Identifiers: chr5:g.136974806A>G (hg19) ; chr5:g.137639117A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.137639117A>G , CM000667.2:g.137639117A>G	GRCh38
NC_000005.9:g.136974806A>G , CM000667.1:g.136974806A>G	GRCh37
NC_000005.8:g.137002705A>G	NCBI36
NG_032569.1:g.101974T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309755.9:c.1055T>C MANE Select	ENSP00000312397.4:p.Val352Ala
ENST00000309755.8:c.1055T>C	ENSP00000312397.4:p.Val352Ala
ENST00000502381.1:n.642T>C
ENST00000504208.5:c.*335-10680T>C	ENSP00000423585.1:n.*335-10680T>C
ENST00000505853.1:c.935T>C	ENSP00000426173.1:p.Val312Ala
ENST00000506491.5:c.809T>C	ENSP00000424828.1:p.Val270Ala
ENST00000506873.5:n.680T>C
ENST00000508657.5:c.959T>C	ENSP00000422099.1:p.Val320Ala
NM_001257194.1:c.959T>C	NP_001244123.1:p.Val320Ala
NM_001257195.1:c.809T>C	NP_001244124.1:p.Val270Ala
NM_017415.2:c.1055T>C	NP_059111.2:p.Val352Ala
NM_017415.3:c.1055T>C MANE Select	NP_059111.2:p.Val352Ala
NM_001257195.2:c.809T>C	NP_001244124.1:p.Val270Ala