Canonical Allele Identifier: CA366981180

Gene: KLHL7

Linked Data

• gnomAD v4: 7-23165737-C-G
• MyVariant Identifiers: chr7:g.23205356C>G (hg19) ; chr7:g.23165737C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.23165737C>G , CM000669.2:g.23165737C>G	GRCh38
NC_000007.13:g.23205356C>G , CM000669.1:g.23205356C>G	GRCh37
NC_000007.12:g.23171881C>G	NCBI36
NG_016983.1:g.65004C>G
NG_016983.2:g.65004C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339077.10:c.976C>G MANE Select	ENSP00000343273.4:p.Arg326Gly
ENST00000339077.9:c.976C>G	ENSP00000343273.4:p.Arg326Gly
ENST00000409689.5:c.832C>G	ENSP00000386263.1:p.Arg278Gly
ENST00000521082.5:c.*984C>G	ENSP00000430351.1:n.*984C>G
NM_001031710.2:c.976C>G	NP_001026880.2:p.Arg326Gly
NM_018846.4:c.832C>G	NP_061334.4:p.Arg278Gly
NR_033328.1:n.1400C>G
XM_006715753.1:c.1015C>G	XP_006715816.1:p.Arg339Gly
XM_006715754.1:c.949C>G	XP_006715817.1:p.Arg317Gly
XM_006715755.1:c.949C>G	XP_006715818.1:p.Arg317Gly
XM_006715756.1:c.871C>G	XP_006715819.1:p.Arg291Gly
XM_006715753.3:c.1015C>G	XP_006715816.1:p.Arg339Gly
XM_006715754.3:c.949C>G	XP_006715817.1:p.Arg317Gly
XM_006715755.3:c.949C>G	XP_006715818.1:p.Arg317Gly
XM_006715756.3:c.871C>G	XP_006715819.1:p.Arg291Gly
XM_017012439.2:c.910C>G	XP_016867928.1:p.Arg304Gly
NM_001031710.3:c.976C>G MANE Select	NP_001026880.2:p.Arg326Gly
NM_018846.5:c.832C>G	NP_061334.4:p.Arg278Gly
NR_033328.2:n.1349C>G