Canonical Allele Identifier: CA1360457312

Gene: KLHL40

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.42688106_42688107delinsTG , CM000665.2:g.42688106_42688107delinsTG	GRCh38
NC_000003.11:g.42729598_42729599delinsTG , CM000665.1:g.42729598_42729599delinsTG	GRCh37
NC_000003.10:g.42704602_42704603delinsTG	NCBI36
NG_033035.1:g.7588_7589delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000287777.5:c.1153-36_1153-35delinsTG MANE Select	ENSP00000287777.4:n.1153-36_1153-35delinsTG
ENST00000287777.4:c.1153-36_1153-35delinsTG	ENSP00000287777.4:n.1153-36_1153-35delinsTG
NM_152393.3:c.1153-36_1153-35delinsTG	NP_689606.2:n.1153-36_1153-35delinsTG
XM_005264866.2:c.1153-36_1153-35delinsTG	XP_005264923.1:n.1153-36_1153-35delinsTG
NM_152393.4:c.1153-36_1153-35delinsTG MANE Select	NP_689606.2:n.1153-36_1153-35delinsTG