Canonical Allele Identifier: CA361045482

Gene: KLHL3

Linked Data

• MyVariant Identifiers: chr5:g.136964024T>G (hg19) ; chr5:g.137628335T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.137628335T>G , CM000667.2:g.137628335T>G	GRCh38
NC_000005.9:g.136964024T>G , CM000667.1:g.136964024T>G	GRCh37
NC_000005.8:g.136991923T>G	NCBI36
NG_032569.1:g.112756A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309755.9:c.1553A>C MANE Select	ENSP00000312397.4:p.Lys518Thr
ENST00000309755.8:c.1553A>C	ENSP00000312397.4:p.Lys518Thr
ENST00000447439.6:n.1609A>C
ENST00000504208.5:c.*437A>C	ENSP00000423585.1:n.*437A>C
ENST00000506491.5:c.1307A>C	ENSP00000424828.1:p.Lys436Thr
ENST00000506873.5:n.1076A>C
ENST00000508657.5:c.1457A>C	ENSP00000422099.1:p.Lys486Thr
ENST00000509694.1:n.346A>C
NM_001257194.1:c.1457A>C	NP_001244123.1:p.Lys486Thr
NM_001257195.1:c.1307A>C	NP_001244124.1:p.Lys436Thr
NM_017415.2:c.1553A>C	NP_059111.2:p.Lys518Thr
NM_017415.3:c.1553A>C MANE Select	NP_059111.2:p.Lys518Thr
NM_001257195.2:c.1307A>C	NP_001244124.1:p.Lys436Thr