Canonical Allele Identifier: CA446560975
Gene: KLHL3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.136974676C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.137638987C>T , CM000667.2:g.137638987C>T GRCh38
NC_000005.9:g.136974676C>T , CM000667.1:g.136974676C>T GRCh37
NC_000005.8:g.137002575C>T NCBI36
NG_032569.1:g.102104G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000309755.9:c.1185G>A MANE Select ENSP00000312397.4:p.Leu395=
ENST00000309755.8:c.1185G>A ENSP00000312397.4:p.Leu395=
ENST00000502381.1:n.772G>A
ENST00000504208.5:c.*335-10550G>A ENSP00000423585.1:n.*335-10550G>A
ENST00000505853.1:c.1065G>A ENSP00000426173.1:p.Leu355=
ENST00000506491.5:c.939G>A ENSP00000424828.1:p.Leu313=
ENST00000506873.5:n.810G>A
ENST00000508657.5:c.1089G>A ENSP00000422099.1:p.Leu363=
NM_001257194.1:c.1089G>A NP_001244123.1:p.Leu363=
NM_001257195.1:c.939G>A NP_001244124.1:p.Leu313=
NM_017415.2:c.1185G>A NP_059111.2:p.Leu395=
NM_017415.3:c.1185G>A MANE Select NP_059111.2:p.Leu395=
NM_001257195.2:c.939G>A NP_001244124.1:p.Leu313=