Canonical Allele Identifier: CA361047931

Gene: KLHL3

Linked Data

• MyVariant Identifiers: chr5:g.136974702G>T (hg19) ; chr5:g.137639013G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.137639013G>T , CM000667.2:g.137639013G>T	GRCh38
NC_000005.9:g.136974702G>T , CM000667.1:g.136974702G>T	GRCh37
NC_000005.8:g.137002601G>T	NCBI36
NG_032569.1:g.102078C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309755.9:c.1159C>A MANE Select	ENSP00000312397.4:p.Leu387Met
ENST00000309755.8:c.1159C>A	ENSP00000312397.4:p.Leu387Met
ENST00000502381.1:n.746C>A
ENST00000504208.5:c.*335-10576C>A	ENSP00000423585.1:n.*335-10576C>A
ENST00000505853.1:c.1039C>A	ENSP00000426173.1:p.Leu347Met
ENST00000506491.5:c.913C>A	ENSP00000424828.1:p.Leu305Met
ENST00000506873.5:n.784C>A
ENST00000508657.5:c.1063C>A	ENSP00000422099.1:p.Leu355Met
NM_001257194.1:c.1063C>A	NP_001244123.1:p.Leu355Met
NM_001257195.1:c.913C>A	NP_001244124.1:p.Leu305Met
NM_017415.2:c.1159C>A	NP_059111.2:p.Leu387Met
NM_017415.3:c.1159C>A MANE Select	NP_059111.2:p.Leu387Met
NM_001257195.2:c.913C>A	NP_001244124.1:p.Leu305Met