Canonical Allele Identifier: CA1585497815

Gene: KLHL3

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.137639223_137639224delinsAG , CM000667.2:g.137639223_137639224delinsAG	GRCh38
NC_000005.9:g.136974912_136974913delinsAG , CM000667.1:g.136974912_136974913delinsAG	GRCh37
NC_000005.8:g.137002811_137002812delinsAG	NCBI36
NG_032569.1:g.101867_101868delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309755.9:c.1022-74_1022-73delinsCT MANE Select	ENSP00000312397.4:n.1022-74_1022-73delinsCT
ENST00000309755.8:c.1022-74_1022-73delinsCT	ENSP00000312397.4:n.1022-74_1022-73delinsCT
ENST00000502381.1:n.609-74_609-73delinsCT
ENST00000504208.5:c.*335-10787_*335-10786delinsCT	ENSP00000423585.1:n.*335-10787_*335-10786delinsCT
ENST00000505853.1:c.902-74_902-73delinsCT	ENSP00000426173.1:n.902-74_902-73delinsCT
ENST00000506491.5:c.776-74_776-73delinsCT	ENSP00000424828.1:n.776-74_776-73delinsCT
ENST00000506873.5:n.647-74_647-73delinsCT
ENST00000508657.5:c.926-74_926-73delinsCT	ENSP00000422099.1:n.926-74_926-73delinsCT
NM_001257194.1:c.926-74_926-73delinsCT	NP_001244123.1:n.926-74_926-73delinsCT
NM_001257195.1:c.776-74_776-73delinsCT	NP_001244124.1:n.776-74_776-73delinsCT
NM_017415.2:c.1022-74_1022-73delinsCT	NP_059111.2:n.1022-74_1022-73delinsCT
NM_017415.3:c.1022-74_1022-73delinsCT MANE Select	NP_059111.2:n.1022-74_1022-73delinsCT
NM_001257195.2:c.776-74_776-73delinsCT	NP_001244124.1:n.776-74_776-73delinsCT