Canonical Allele Identifier: CA1694330806

Gene: KLHL7

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.23165883C= , CM000669.2:g.23165883C=	GRCh38
NC_000007.13:g.23205502C= , CM000669.1:g.23205502C=	GRCh37
NC_000007.12:g.23172027C=	NCBI36
NG_016983.1:g.65150C=
NG_016983.2:g.65150C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339077.10:c.1122C= MANE Select	ENSP00000343273.4:p.Ser374=
ENST00000339077.9:c.1122C=	ENSP00000343273.4:p.Ser374=
ENST00000409689.5:c.978C=	ENSP00000386263.1:p.Ser326=
ENST00000469576.1:n.9C=
ENST00000521082.5:c.*1130C=	ENSP00000430351.1:n.*1130C=
NM_001031710.2:c.1122C=	NP_001026880.2:p.Ser374=
NM_018846.4:c.978C=	NP_061334.4:p.Ser326=
NR_033328.1:n.1546C=
XM_006715753.1:c.1161C=	XP_006715816.1:p.Ser387=
XM_006715754.1:c.1095C=	XP_006715817.1:p.Ser365=
XM_006715755.1:c.1095C=	XP_006715818.1:p.Ser365=
XM_006715756.1:c.1017C=	XP_006715819.1:p.Ser339=
XM_006715753.3:c.1161C=	XP_006715816.1:p.Ser387=
XM_006715754.3:c.1095C=	XP_006715817.1:p.Ser365=
XM_006715755.3:c.1095C=	XP_006715818.1:p.Ser365=
XM_006715756.3:c.1017C=	XP_006715819.1:p.Ser339=
XM_017012439.2:c.1056C=	XP_016867928.1:p.Ser352=
NM_001031710.3:c.1122C= MANE Select	NP_001026880.2:p.Ser374=
NM_018846.5:c.978C=	NP_061334.4:p.Ser326=
NR_033328.2:n.1495C=