Canonical Allele Identifier: CA1585497518
Gene: KLHL3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.137639000A= , CM000667.2:g.137639000A= GRCh38
NC_000005.9:g.136974689A= , CM000667.1:g.136974689A= GRCh37
NC_000005.8:g.137002588A= NCBI36
NG_032569.1:g.102091T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000309755.9:c.1172T= MANE Select ENSP00000312397.4:p.Val391=
ENST00000309755.8:c.1172T= ENSP00000312397.4:p.Val391=
ENST00000502381.1:n.759T=
ENST00000504208.5:c.*335-10563T= ENSP00000423585.1:n.*335-10563T=
ENST00000505853.1:c.1052T= ENSP00000426173.1:p.Val351=
ENST00000506491.5:c.926T= ENSP00000424828.1:p.Val309=
ENST00000506873.5:n.797T=
ENST00000508657.5:c.1076T= ENSP00000422099.1:p.Val359=
NM_001257194.1:c.1076T= NP_001244123.1:p.Val359=
NM_001257195.1:c.926T= NP_001244124.1:p.Val309=
NM_017415.2:c.1172T= NP_059111.2:p.Val391=
NM_017415.3:c.1172T= MANE Select NP_059111.2:p.Val391=
NM_001257195.2:c.926T= NP_001244124.1:p.Val309=