Canonical Allele Identifier: CA1360457356
Gene: KLHL40 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.42688175C= , CM000665.2:g.42688175C= GRCh38
NC_000003.11:g.42729667C= , CM000665.1:g.42729667C= GRCh37
NC_000003.10:g.42704671C= NCBI36
NG_033035.1:g.7657C=

Transcript Alleles

HGVS Amino-acid change
ENST00000287777.5:c.1186C= MANE Select ENSP00000287777.4:p.Pro396=
ENST00000287777.4:c.1186C= ENSP00000287777.4:p.Pro396=
NM_152393.3:c.1186C= NP_689606.2:p.Pro396=
XM_005264866.2:c.1186C= XP_005264923.1:p.Pro396=
NM_152393.4:c.1186C= MANE Select NP_689606.2:p.Pro396=