Canonical Allele Identifier: CA1694330761

Gene: KLHL7

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.23165703T= , CM000669.2:g.23165703T=	GRCh38
NC_000007.13:g.23205322T= , CM000669.1:g.23205322T=	GRCh37
NC_000007.12:g.23171847T=	NCBI36
NG_016983.1:g.64970T=
NG_016983.2:g.64970T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339077.10:c.942T= MANE Select	ENSP00000343273.4:p.Tyr314=
ENST00000339077.9:c.942T=	ENSP00000343273.4:p.Tyr314=
ENST00000409689.5:c.798T=	ENSP00000386263.1:p.Tyr266=
ENST00000521082.5:c.*950T=	ENSP00000430351.1:n.*950T=
NM_001031710.2:c.942T=	NP_001026880.2:p.Tyr314=
NM_018846.4:c.798T=	NP_061334.4:p.Tyr266=
NR_033328.1:n.1366T=
XM_006715753.1:c.981T=	XP_006715816.1:p.Tyr327=
XM_006715754.1:c.915T=	XP_006715817.1:p.Tyr305=
XM_006715755.1:c.915T=	XP_006715818.1:p.Tyr305=
XM_006715756.1:c.837T=	XP_006715819.1:p.Tyr279=
XM_006715753.3:c.981T=	XP_006715816.1:p.Tyr327=
XM_006715754.3:c.915T=	XP_006715817.1:p.Tyr305=
XM_006715755.3:c.915T=	XP_006715818.1:p.Tyr305=
XM_006715756.3:c.837T=	XP_006715819.1:p.Tyr279=
XM_017012439.2:c.876T=	XP_016867928.1:p.Tyr292=
NM_001031710.3:c.942T= MANE Select	NP_001026880.2:p.Tyr314=
NM_018846.5:c.798T=	NP_061334.4:p.Tyr266=
NR_033328.2:n.1315T=