Canonical Allele Identifier: CA1694335276

Gene: KLHL7

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.23167826T= , CM000669.2:g.23167826T=	GRCh38
NC_000007.13:g.23207445T= , CM000669.1:g.23207445T=	GRCh37
NC_000007.12:g.23173970T=	NCBI36
NG_016983.1:g.67093T=
NG_016983.2:g.67093T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339077.10:c.1178-10T= MANE Select	ENSP00000343273.4:n.1178-10T=
ENST00000339077.9:c.1178-10T=	ENSP00000343273.4:n.1178-10T=
ENST00000409689.5:c.1034-10T=	ENSP00000386263.1:n.1034-10T=
ENST00000469576.1:n.65-10T=
ENST00000521082.5:c.*1186-10T=	ENSP00000430351.1:n.*1186-10T=
NM_001031710.2:c.1178-10T=	NP_001026880.2:n.1178-10T=
NM_018846.4:c.1034-10T=	NP_061334.4:n.1034-10T=
NR_033328.1:n.1602-10T=
XM_006715753.1:c.1217-10T=	XP_006715816.1:n.1217-10T=
XM_006715754.1:c.1151-10T=	XP_006715817.1:n.1151-10T=
XM_006715755.1:c.1151-10T=	XP_006715818.1:n.1151-10T=
XM_006715756.1:c.1073-10T=	XP_006715819.1:n.1073-10T=
XM_006715753.3:c.1217-10T=	XP_006715816.1:n.1217-10T=
XM_006715754.3:c.1151-10T=	XP_006715817.1:n.1151-10T=
XM_006715755.3:c.1151-10T=	XP_006715818.1:n.1151-10T=
XM_006715756.3:c.1073-10T=	XP_006715819.1:n.1073-10T=
XM_017012439.2:c.1112-10T=	XP_016867928.1:n.1112-10T=
NM_001031710.3:c.1178-10T= MANE Select	NP_001026880.2:n.1178-10T=
NM_018846.5:c.1034-10T=	NP_061334.4:n.1034-10T=
NR_033328.2:n.1551-10T=