Canonical Allele Identifier: CA1360457342
Gene: KLHL40 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.42688149A= , CM000665.2:g.42688149A= GRCh38
NC_000003.11:g.42729641A= , CM000665.1:g.42729641A= GRCh37
NC_000003.10:g.42704645A= NCBI36
NG_033035.1:g.7631A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000287777.5:c.1160A= MANE Select ENSP00000287777.4:p.His387=
ENST00000287777.4:c.1160A= ENSP00000287777.4:p.His387=
NM_152393.3:c.1160A= NP_689606.2:p.His387=
XM_005264866.2:c.1160A= XP_005264923.1:p.His387=
NM_152393.4:c.1160A= MANE Select NP_689606.2:p.His387=
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