Canonical Allele Identifier: CA1360457365
Gene: KLHL40 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.42688186C= , CM000665.2:g.42688186C= GRCh38
NC_000003.11:g.42729678C= , CM000665.1:g.42729678C= GRCh37
NC_000003.10:g.42704682C= NCBI36
NG_033035.1:g.7668C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000287777.5:c.1197C= MANE Select ENSP00000287777.4:p.Pro399=
ENST00000287777.4:c.1197C= ENSP00000287777.4:p.Pro399=
NM_152393.3:c.1197C= NP_689606.2:p.Pro399=
XM_005264866.2:c.1197C= XP_005264923.1:p.Pro399=
NM_152393.4:c.1197C= MANE Select NP_689606.2:p.Pro399=
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