Canonical Allele Identifier: CA1585515251
Gene: KLHL3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.137637317C= , CM000667.2:g.137637317C= GRCh38
NC_000005.9:g.136973006C= , CM000667.1:g.136973006C= GRCh37
NC_000005.8:g.137000905C= NCBI36
NG_032569.1:g.103774G=

Transcript Alleles

HGVS Amino-acid Change
NM_017415.3:c.1298G= MANE Select NP_059111.2:p.Ser433=
ENST00000309755.9:c.1298G= MANE Select ENSP00000312397.4:p.Ser433=
NM_001257194.1:c.1202G= NP_001244123.1:p.Ser401=
NM_001257195.1:c.1052G= NP_001244124.1:p.Ser351=
NM_001257195.2:c.1052G= NP_001244124.1:p.Ser351=
NM_017415.2:c.1298G= NP_059111.2:p.Ser433=
ENST00000309755.8:c.1298G= ENSP00000312397.4:p.Ser433=
ENST00000502381.1:n.806+1636G=
ENST00000504208.5:c.*335-8880G= ENSP00000423585.1:n.*335-8880G=
ENST00000505853.1:c.1178G= ENSP00000426173.1:p.Ser393=
ENST00000506491.5:c.1052G= ENSP00000424828.1:p.Ser351=
ENST00000506873.5:n.844+1636G=
ENST00000508657.5:c.1202G= ENSP00000422099.1:p.Ser401=