Canonical Allele Identifier: CA1585515840
Gene: KLHL3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.137638771T= , CM000667.2:g.137638771T= GRCh38
NC_000005.9:g.136974460T= , CM000667.1:g.136974460T= GRCh37
NC_000005.8:g.137002359T= NCBI36
NG_032569.1:g.102320A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000309755.9:c.1219+182A= MANE Select ENSP00000312397.4:n.1219+182A=
ENST00000309755.8:c.1219+182A= ENSP00000312397.4:n.1219+182A=
ENST00000502381.1:n.806+182A=
ENST00000504208.5:c.*335-10334A= ENSP00000423585.1:n.*335-10334A=
ENST00000505853.1:c.1099+182A= ENSP00000426173.1:n.1099+182A=
ENST00000506491.5:c.973+182A= ENSP00000424828.1:n.973+182A=
ENST00000506873.5:n.844+182A=
ENST00000508657.5:c.1123+182A= ENSP00000422099.1:n.1123+182A=
NM_001257194.1:c.1123+182A= NP_001244123.1:n.1123+182A=
NM_001257195.1:c.973+182A= NP_001244124.1:n.973+182A=
NM_017415.2:c.1219+182A= NP_059111.2:n.1219+182A=
NM_017415.3:c.1219+182A= MANE Select NP_059111.2:n.1219+182A=
NM_001257195.2:c.973+182A= NP_001244124.1:n.973+182A=