Canonical Allele Identifier: CA1585497588
Gene: KLHL3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.137639053C= , CM000667.2:g.137639053C= GRCh38
NC_000005.9:g.136974742C= , CM000667.1:g.136974742C= GRCh37
NC_000005.8:g.137002641C= NCBI36
NG_032569.1:g.102038G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000309755.9:c.1119G= MANE Select ENSP00000312397.4:p.Gln373=
ENST00000309755.8:c.1119G= ENSP00000312397.4:p.Gln373=
ENST00000502381.1:n.706G=
ENST00000504208.5:c.*335-10616G= ENSP00000423585.1:n.*335-10616G=
ENST00000505853.1:c.999G= ENSP00000426173.1:p.Gln333=
ENST00000506491.5:c.873G= ENSP00000424828.1:p.Gln291=
ENST00000506873.5:n.744G=
ENST00000508657.5:c.1023G= ENSP00000422099.1:p.Gln341=
NM_001257194.1:c.1023G= NP_001244123.1:p.Gln341=
NM_001257195.1:c.873G= NP_001244124.1:p.Gln291=
NM_017415.2:c.1119G= NP_059111.2:p.Gln373=
NM_017415.3:c.1119G= MANE Select NP_059111.2:p.Gln373=
NM_001257195.2:c.873G= NP_001244124.1:p.Gln291=