Canonical Allele Identifier: CA11004036

Gene: KLHL29

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.23675447C>T , CM000664.2:g.23675447C>T	GRCh38
NC_000002.11:g.23898317C>T , CM000664.1:g.23898317C>T	GRCh37
NC_000002.10:g.23751822C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000486442.6:c.941-8952C>T MANE Select	ENSP00000420659.1:n.941-8952C>T
ENST00000288548.5:c.460-8952C>T
ENST00000486442.5:c.941-8952C>T	ENSP00000420659.1:n.941-8952C>T
NM_052920.1:c.941-8952C>T	NP_443152.1:n.941-8952C>T
XM_006711929.2:c.941-8952C>T	XP_006711992.1:n.941-8952C>T
XM_011532501.1:c.23-8952C>T	XP_011530803.1:n.23-8952C>T
XM_006711929.3:c.941-8952C>T	XP_006711992.1:n.941-8952C>T
XM_011532501.2:c.23-8952C>T	XP_011530803.1:n.23-8952C>T
XM_017003264.2:c.941-8952C>T	XP_016858753.1:n.941-8952C>T
NM_052920.2:c.941-8952C>T MANE Select	NP_443152.1:n.941-8952C>T