Canonical Allele Identifier: CA352293564

Gene: KLHL40

Linked Data

• MyVariant Identifiers: chr3:g.42729750G>T (hg19) ; chr3:g.42688258G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.42688258G>T , CM000665.2:g.42688258G>T	GRCh38
NC_000003.11:g.42729750G>T , CM000665.1:g.42729750G>T	GRCh37
NC_000003.10:g.42704754G>T	NCBI36
NG_033035.1:g.7740G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000287777.5:c.1269G>T MANE Select	ENSP00000287777.4:p.Lys423Asn
ENST00000287777.4:c.1269G>T	ENSP00000287777.4:p.Lys423Asn
NM_152393.3:c.1269G>T	NP_689606.2:p.Lys423Asn
XM_005264866.2:c.1269G>T	XP_005264923.1:p.Lys423Asn
NM_152393.4:c.1269G>T MANE Select	NP_689606.2:p.Lys423Asn