Canonical Allele Identifier: CA1694330783

Gene: KLHL7

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.23165780T= , CM000669.2:g.23165780T=	GRCh38
NC_000007.13:g.23205399T= , CM000669.1:g.23205399T=	GRCh37
NC_000007.12:g.23171924T=	NCBI36
NG_016983.1:g.65047T=
NG_016983.2:g.65047T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000339077.10:c.1019T= MANE Select	ENSP00000343273.4:p.Ile340=
ENST00000339077.9:c.1019T=	ENSP00000343273.4:p.Ile340=
ENST00000409689.5:c.875T=	ENSP00000386263.1:p.Ile292=
ENST00000521082.5:c.*1027T=	ENSP00000430351.1:n.*1027T=
NM_001031710.2:c.1019T=	NP_001026880.2:p.Ile340=
NM_018846.4:c.875T=	NP_061334.4:p.Ile292=
NR_033328.1:n.1443T=
XM_006715753.1:c.1058T=	XP_006715816.1:p.Ile353=
XM_006715754.1:c.992T=	XP_006715817.1:p.Ile331=
XM_006715755.1:c.992T=	XP_006715818.1:p.Ile331=
XM_006715756.1:c.914T=	XP_006715819.1:p.Ile305=
XM_006715753.3:c.1058T=	XP_006715816.1:p.Ile353=
XM_006715754.3:c.992T=	XP_006715817.1:p.Ile331=
XM_006715755.3:c.992T=	XP_006715818.1:p.Ile331=
XM_006715756.3:c.914T=	XP_006715819.1:p.Ile305=
XM_017012439.2:c.953T=	XP_016867928.1:p.Ile318=
NM_001031710.3:c.1019T= MANE Select	NP_001026880.2:p.Ile340=
NM_018846.5:c.875T=	NP_061334.4:p.Ile292=
NR_033328.2:n.1392T=