Canonical Allele Identifier: CA446556390

Gene: KLHL3

Linked Data

• MyVariant Identifiers: chr5:g.136964101C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.137628412C>A , CM000667.2:g.137628412C>A	GRCh38
NC_000005.9:g.136964101C>A , CM000667.1:g.136964101C>A	GRCh37
NC_000005.8:g.136992000C>A	NCBI36
NG_032569.1:g.112679G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309755.9:c.1476G>T MANE Select	ENSP00000312397.4:p.Leu492=
ENST00000309755.8:c.1476G>T	ENSP00000312397.4:p.Leu492=
ENST00000447439.6:n.1532G>T
ENST00000504208.5:c.*360G>T	ENSP00000423585.1:n.*360G>T
ENST00000506491.5:c.1230G>T	ENSP00000424828.1:p.Leu410=
ENST00000506873.5:n.999G>T
ENST00000508657.5:c.1380G>T	ENSP00000422099.1:p.Leu460=
ENST00000509694.1:n.269G>T
NM_001257194.1:c.1380G>T	NP_001244123.1:p.Leu460=
NM_001257195.1:c.1230G>T	NP_001244124.1:p.Leu410=
NM_017415.2:c.1476G>T	NP_059111.2:p.Leu492=
NM_017415.3:c.1476G>T MANE Select	NP_059111.2:p.Leu492=
NM_001257195.2:c.1230G>T	NP_001244124.1:p.Leu410=