Canonical Allele Identifier: CA446561113
Gene: KLHL3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.136974787T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.137639098T>A , CM000667.2:g.137639098T>A GRCh38
NC_000005.9:g.136974787T>A , CM000667.1:g.136974787T>A GRCh37
NC_000005.8:g.137002686T>A NCBI36
NG_032569.1:g.101993A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000309755.9:c.1074A>T MANE Select ENSP00000312397.4:p.Ser358=
ENST00000309755.8:c.1074A>T ENSP00000312397.4:p.Ser358=
ENST00000502381.1:n.661A>T
ENST00000504208.5:c.*335-10661A>T ENSP00000423585.1:n.*335-10661A>T
ENST00000505853.1:c.954A>T ENSP00000426173.1:p.Ser318=
ENST00000506491.5:c.828A>T ENSP00000424828.1:p.Ser276=
ENST00000506873.5:n.699A>T
ENST00000508657.5:c.978A>T ENSP00000422099.1:p.Ser326=
NM_001257194.1:c.978A>T NP_001244123.1:p.Ser326=
NM_001257195.1:c.828A>T NP_001244124.1:p.Ser276=
NM_017415.2:c.1074A>T NP_059111.2:p.Ser358=
NM_017415.3:c.1074A>T MANE Select NP_059111.2:p.Ser358=
NM_001257195.2:c.828A>T NP_001244124.1:p.Ser276=