Canonical Allele Identifier: CA366981608

Gene: KLHL7

Linked Data

• ClinVar Variation Id: 2248752
• ClinVar RCV Id: RCV002752584
• MyVariant Identifiers: chr7:g.23205545G>A (hg19) ; chr7:g.23165926G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.23165926G>A , CM000669.2:g.23165926G>A	GRCh38
NC_000007.13:g.23205545G>A , CM000669.1:g.23205545G>A	GRCh37
NC_000007.12:g.23172070G>A	NCBI36
NG_016983.1:g.65193G>A
NG_016983.2:g.65193G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339077.10:c.1165G>A MANE Select	ENSP00000343273.4:p.Gly389Ser
ENST00000339077.9:c.1165G>A	ENSP00000343273.4:p.Gly389Ser
ENST00000409689.5:c.1021G>A	ENSP00000386263.1:p.Gly341Ser
ENST00000469576.1:n.52G>A
ENST00000521082.5:c.*1173G>A	ENSP00000430351.1:n.*1173G>A
NM_001031710.2:c.1165G>A	NP_001026880.2:p.Gly389Ser
NM_018846.4:c.1021G>A	NP_061334.4:p.Gly341Ser
NR_033328.1:n.1589G>A
XM_006715753.1:c.1204G>A	XP_006715816.1:p.Gly402Ser
XM_006715754.1:c.1138G>A	XP_006715817.1:p.Gly380Ser
XM_006715755.1:c.1138G>A	XP_006715818.1:p.Gly380Ser
XM_006715756.1:c.1060G>A	XP_006715819.1:p.Gly354Ser
XM_006715753.3:c.1204G>A	XP_006715816.1:p.Gly402Ser
XM_006715754.3:c.1138G>A	XP_006715817.1:p.Gly380Ser
XM_006715755.3:c.1138G>A	XP_006715818.1:p.Gly380Ser
XM_006715756.3:c.1060G>A	XP_006715819.1:p.Gly354Ser
XM_017012439.2:c.1099G>A	XP_016867928.1:p.Gly367Ser
NM_001031710.3:c.1165G>A MANE Select	NP_001026880.2:p.Gly389Ser
NM_018846.5:c.1021G>A	NP_061334.4:p.Gly341Ser
NR_033328.2:n.1538G>A