Canonical Allele Identifier: CA446561008
Gene: KLHL3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.136974700C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.137639011C>G , CM000667.2:g.137639011C>G GRCh38
NC_000005.9:g.136974700C>G , CM000667.1:g.136974700C>G GRCh37
NC_000005.8:g.137002599C>G NCBI36
NG_032569.1:g.102080G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000309755.9:c.1161G>C MANE Select ENSP00000312397.4:p.Leu387=
ENST00000309755.8:c.1161G>C ENSP00000312397.4:p.Leu387=
ENST00000502381.1:n.748G>C
ENST00000504208.5:c.*335-10574G>C ENSP00000423585.1:n.*335-10574G>C
ENST00000505853.1:c.1041G>C ENSP00000426173.1:p.Leu347=
ENST00000506491.5:c.915G>C ENSP00000424828.1:p.Leu305=
ENST00000506873.5:n.786G>C
ENST00000508657.5:c.1065G>C ENSP00000422099.1:p.Leu355=
NM_001257194.1:c.1065G>C NP_001244123.1:p.Leu355=
NM_001257195.1:c.915G>C NP_001244124.1:p.Leu305=
NM_017415.2:c.1161G>C NP_059111.2:p.Leu387=
NM_017415.3:c.1161G>C MANE Select NP_059111.2:p.Leu387=
NM_001257195.2:c.915G>C NP_001244124.1:p.Leu305=