Canonical Allele Identifier: CA1585498500
Gene: KLHL3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.137639955T= , CM000667.2:g.137639955T= GRCh38
NC_000005.9:g.136975644T= , CM000667.1:g.136975644T= GRCh37
NC_000005.8:g.137003543T= NCBI36
NG_032569.1:g.101136A=

Transcript Alleles

HGVS Amino-acid change
ENST00000309755.9:c.926A= MANE Select ENSP00000312397.4:p.Gln309=
ENST00000309755.8:c.926A= ENSP00000312397.4:p.Gln309=
ENST00000502381.1:n.513A=
ENST00000504208.5:c.*335-11518A= ENSP00000423585.1:n.*335-11518A=
ENST00000505853.1:c.806A= ENSP00000426173.1:p.Gln269=
ENST00000506491.5:c.680A= ENSP00000424828.1:p.Gln227=
ENST00000506873.5:n.551A=
ENST00000508657.5:c.830A= ENSP00000422099.1:p.Gln277=
NM_001257194.1:c.830A= NP_001244123.1:p.Gln277=
NM_001257195.1:c.680A= NP_001244124.1:p.Gln227=
NM_017415.2:c.926A= NP_059111.2:p.Gln309=
NM_017415.3:c.926A= MANE Select NP_059111.2:p.Gln309=
NM_001257195.2:c.680A= NP_001244124.1:p.Gln227=