Canonical Allele Identifier: CA1585515930
Gene: KLHL3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.137638954A= , CM000667.2:g.137638954A= GRCh38
NC_000005.9:g.136974643A= , CM000667.1:g.136974643A= GRCh37
NC_000005.8:g.137002542A= NCBI36
NG_032569.1:g.102137T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000309755.9:c.1218T= MANE Select ENSP00000312397.4:p.Thr406=
ENST00000309755.8:c.1218T= ENSP00000312397.4:p.Thr406=
ENST00000502381.1:n.805T=
ENST00000504208.5:c.*335-10517T= ENSP00000423585.1:n.*335-10517T=
ENST00000505853.1:c.1098T= ENSP00000426173.1:p.Thr366=
ENST00000506491.5:c.972T= ENSP00000424828.1:p.Thr324=
ENST00000506873.5:n.843T=
ENST00000508657.5:c.1122T= ENSP00000422099.1:p.Thr374=
NM_001257194.1:c.1122T= NP_001244123.1:p.Thr374=
NM_001257195.1:c.972T= NP_001244124.1:p.Thr324=
NM_017415.2:c.1218T= NP_059111.2:p.Thr406=
NM_017415.3:c.1218T= MANE Select NP_059111.2:p.Thr406=
NM_001257195.2:c.972T= NP_001244124.1:p.Thr324=