Canonical Allele Identifier: CA446561043
Gene: KLHL3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.136974733G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.137639044G>C , CM000667.2:g.137639044G>C GRCh38
NC_000005.9:g.136974733G>C , CM000667.1:g.136974733G>C GRCh37
NC_000005.8:g.137002632G>C NCBI36
NG_032569.1:g.102047C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000309755.9:c.1128C>G MANE Select ENSP00000312397.4:p.Ser376=
ENST00000309755.8:c.1128C>G ENSP00000312397.4:p.Ser376=
ENST00000502381.1:n.715C>G
ENST00000504208.5:c.*335-10607C>G ENSP00000423585.1:n.*335-10607C>G
ENST00000505853.1:c.1008C>G ENSP00000426173.1:p.Ser336=
ENST00000506491.5:c.882C>G ENSP00000424828.1:p.Ser294=
ENST00000506873.5:n.753C>G
ENST00000508657.5:c.1032C>G ENSP00000422099.1:p.Ser344=
NM_001257194.1:c.1032C>G NP_001244123.1:p.Ser344=
NM_001257195.1:c.882C>G NP_001244124.1:p.Ser294=
NM_017415.2:c.1128C>G NP_059111.2:p.Ser376=
NM_017415.3:c.1128C>G MANE Select NP_059111.2:p.Ser376=
NM_001257195.2:c.882C>G NP_001244124.1:p.Ser294=