Canonical Allele Identifier: CA1694330777

Gene: KLHL7

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.23165755G= , CM000669.2:g.23165755G=	GRCh38
NC_000007.13:g.23205374G= , CM000669.1:g.23205374G=	GRCh37
NC_000007.12:g.23171899G=	NCBI36
NG_016983.1:g.65022G=
NG_016983.2:g.65022G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339077.10:c.994G= MANE Select	ENSP00000343273.4:p.Val332=
ENST00000339077.9:c.994G=	ENSP00000343273.4:p.Val332=
ENST00000409689.5:c.850G=	ENSP00000386263.1:p.Val284=
ENST00000521082.5:c.*1002G=	ENSP00000430351.1:n.*1002G=
NM_001031710.2:c.994G=	NP_001026880.2:p.Val332=
NM_018846.4:c.850G=	NP_061334.4:p.Val284=
NR_033328.1:n.1418G=
XM_006715753.1:c.1033G=	XP_006715816.1:p.Val345=
XM_006715754.1:c.967G=	XP_006715817.1:p.Val323=
XM_006715755.1:c.967G=	XP_006715818.1:p.Val323=
XM_006715756.1:c.889G=	XP_006715819.1:p.Val297=
XM_006715753.3:c.1033G=	XP_006715816.1:p.Val345=
XM_006715754.3:c.967G=	XP_006715817.1:p.Val323=
XM_006715755.3:c.967G=	XP_006715818.1:p.Val323=
XM_006715756.3:c.889G=	XP_006715819.1:p.Val297=
XM_017012439.2:c.928G=	XP_016867928.1:p.Val310=
NM_001031710.3:c.994G= MANE Select	NP_001026880.2:p.Val332=
NM_018846.5:c.850G=	NP_061334.4:p.Val284=
NR_033328.2:n.1367G=