Canonical Allele Identifier: CA433210592
Gene: KLHL40 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.42729663G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.42688171G>A , CM000665.2:g.42688171G>A GRCh38
NC_000003.11:g.42729663G>A , CM000665.1:g.42729663G>A GRCh37
NC_000003.10:g.42704667G>A NCBI36
NG_033035.1:g.7653G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000287777.5:c.1182G>A MANE Select ENSP00000287777.4:p.Gly394=
ENST00000287777.4:c.1182G>A ENSP00000287777.4:p.Gly394=
NM_152393.3:c.1182G>A NP_689606.2:p.Gly394=
XM_005264866.2:c.1182G>A XP_005264923.1:p.Gly394=
NM_152393.4:c.1182G>A MANE Select NP_689606.2:p.Gly394=
Search 100 bp 5'
Search 100 bp 3'