Canonical Allele Identifier: CA1694330817

Gene: KLHL7

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.23165923G= , CM000669.2:g.23165923G=	GRCh38
NC_000007.13:g.23205542G= , CM000669.1:g.23205542G=	GRCh37
NC_000007.12:g.23172067G=	NCBI36
NG_016983.1:g.65190G=
NG_016983.2:g.65190G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339077.10:c.1162G= MANE Select	ENSP00000343273.4:p.Gly388=
ENST00000339077.9:c.1162G=	ENSP00000343273.4:p.Gly388=
ENST00000409689.5:c.1018G=	ENSP00000386263.1:p.Gly340=
ENST00000469576.1:n.49G=
ENST00000521082.5:c.*1170G=	ENSP00000430351.1:n.*1170G=
NM_001031710.2:c.1162G=	NP_001026880.2:p.Gly388=
NM_018846.4:c.1018G=	NP_061334.4:p.Gly340=
NR_033328.1:n.1586G=
XM_006715753.1:c.1201G=	XP_006715816.1:p.Gly401=
XM_006715754.1:c.1135G=	XP_006715817.1:p.Gly379=
XM_006715755.1:c.1135G=	XP_006715818.1:p.Gly379=
XM_006715756.1:c.1057G=	XP_006715819.1:p.Gly353=
XM_006715753.3:c.1201G=	XP_006715816.1:p.Gly401=
XM_006715754.3:c.1135G=	XP_006715817.1:p.Gly379=
XM_006715755.3:c.1135G=	XP_006715818.1:p.Gly379=
XM_006715756.3:c.1057G=	XP_006715819.1:p.Gly353=
XM_017012439.2:c.1096G=	XP_016867928.1:p.Gly366=
NM_001031710.3:c.1162G= MANE Select	NP_001026880.2:p.Gly388=
NM_018846.5:c.1018G=	NP_061334.4:p.Gly340=
NR_033328.2:n.1535G=