Canonical Allele Identifier: CA1585511485
Gene: KLHL3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.137628458T= , CM000667.2:g.137628458T= GRCh38
NC_000005.9:g.136964147T= , CM000667.1:g.136964147T= GRCh37
NC_000005.8:g.136992046T= NCBI36
NG_032569.1:g.112633A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000309755.9:c.1451-21A= MANE Select ENSP00000312397.4:n.1451-21A=
ENST00000309755.8:c.1451-21A= ENSP00000312397.4:n.1451-21A=
ENST00000447439.6:n.1486A=
ENST00000504208.5:c.*335-21A= ENSP00000423585.1:n.*335-21A=
ENST00000506491.5:c.1205-21A= ENSP00000424828.1:n.1205-21A=
ENST00000506873.5:n.974-21A=
ENST00000508657.5:c.1355-21A= ENSP00000422099.1:n.1355-21A=
ENST00000509694.1:n.223A=
NM_001257194.1:c.1355-21A= NP_001244123.1:n.1355-21A=
NM_001257195.1:c.1205-21A= NP_001244124.1:n.1205-21A=
NM_017415.2:c.1451-21A= NP_059111.2:n.1451-21A=
NM_017415.3:c.1451-21A= MANE Select NP_059111.2:n.1451-21A=
NM_001257195.2:c.1205-21A= NP_001244124.1:n.1205-21A=