Canonical Allele Identifier: CA352293562

Gene: KLHL40

Linked Data

• MyVariant Identifiers: chr3:g.42729749A>T (hg19) ; chr3:g.42688257A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.42688257A>T , CM000665.2:g.42688257A>T	GRCh38
NC_000003.11:g.42729749A>T , CM000665.1:g.42729749A>T	GRCh37
NC_000003.10:g.42704753A>T	NCBI36
NG_033035.1:g.7739A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000287777.5:c.1268A>T MANE Select	ENSP00000287777.4:p.Lys423Met
ENST00000287777.4:c.1268A>T	ENSP00000287777.4:p.Lys423Met
NM_152393.3:c.1268A>T	NP_689606.2:p.Lys423Met
XM_005264866.2:c.1268A>T	XP_005264923.1:p.Lys423Met
NM_152393.4:c.1268A>T MANE Select	NP_689606.2:p.Lys423Met