Canonical Allele Identifier: CA366981621

Gene: KLHL7

Linked Data

• MyVariant Identifiers: chr7:g.23205551G>C (hg19) ; chr7:g.23165932G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.23165932G>C , CM000669.2:g.23165932G>C	GRCh38
NC_000007.13:g.23205551G>C , CM000669.1:g.23205551G>C	GRCh37
NC_000007.12:g.23172076G>C	NCBI36
NG_016983.1:g.65199G>C
NG_016983.2:g.65199G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339077.10:c.1171G>C MANE Select	ENSP00000343273.4:p.Glu391Gln
ENST00000339077.9:c.1171G>C	ENSP00000343273.4:p.Glu391Gln
ENST00000409689.5:c.1027G>C	ENSP00000386263.1:p.Glu343Gln
ENST00000469576.1:n.58G>C
ENST00000521082.5:c.*1179G>C	ENSP00000430351.1:n.*1179G>C
NM_001031710.2:c.1171G>C	NP_001026880.2:p.Glu391Gln
NM_018846.4:c.1027G>C	NP_061334.4:p.Glu343Gln
NR_033328.1:n.1595G>C
XM_006715753.1:c.1210G>C	XP_006715816.1:p.Glu404Gln
XM_006715754.1:c.1144G>C	XP_006715817.1:p.Glu382Gln
XM_006715755.1:c.1144G>C	XP_006715818.1:p.Glu382Gln
XM_006715756.1:c.1066G>C	XP_006715819.1:p.Glu356Gln
XM_006715753.3:c.1210G>C	XP_006715816.1:p.Glu404Gln
XM_006715754.3:c.1144G>C	XP_006715817.1:p.Glu382Gln
XM_006715755.3:c.1144G>C	XP_006715818.1:p.Glu382Gln
XM_006715756.3:c.1066G>C	XP_006715819.1:p.Glu356Gln
XM_017012439.2:c.1105G>C	XP_016867928.1:p.Glu369Gln
NM_001031710.3:c.1171G>C MANE Select	NP_001026880.2:p.Glu391Gln
NM_018846.5:c.1027G>C	NP_061334.4:p.Glu343Gln
NR_033328.2:n.1544G>C