Canonical Allele Identifier: CA446560934
Gene: KLHL3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.136974646A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.137638957A>G , CM000667.2:g.137638957A>G GRCh38
NC_000005.9:g.136974646A>G , CM000667.1:g.136974646A>G GRCh37
NC_000005.8:g.137002545A>G NCBI36
NG_032569.1:g.102134T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000309755.9:c.1215T>C MANE Select ENSP00000312397.4:p.Ser405=
ENST00000309755.8:c.1215T>C ENSP00000312397.4:p.Ser405=
ENST00000502381.1:n.802T>C
ENST00000504208.5:c.*335-10520T>C ENSP00000423585.1:n.*335-10520T>C
ENST00000505853.1:c.1095T>C ENSP00000426173.1:p.Ser365=
ENST00000506491.5:c.969T>C ENSP00000424828.1:p.Ser323=
ENST00000506873.5:n.840T>C
ENST00000508657.5:c.1119T>C ENSP00000422099.1:p.Ser373=
NM_001257194.1:c.1119T>C NP_001244123.1:p.Ser373=
NM_001257195.1:c.969T>C NP_001244124.1:p.Ser323=
NM_017415.2:c.1215T>C NP_059111.2:p.Ser405=
NM_017415.3:c.1215T>C MANE Select NP_059111.2:p.Ser405=
NM_001257195.2:c.969T>C NP_001244124.1:p.Ser323=