Canonical Allele Identifier: CA1694330779
Gene: KLHL7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.23165759_23165775delinsTTTGGGACAATGTAGTA , CM000669.2:g.23165759_23165775delinsTTTGGGACAATGTAGTA GRCh38
NC_000007.13:g.23205378_23205394delinsTTTGGGACAATGTAGTA , CM000669.1:g.23205378_23205394delinsTTTGGGACAATGTAGTA GRCh37
NC_000007.12:g.23171903_23171919delinsTTTGGGACAATGTAGTA NCBI36
NG_016983.1:g.65026_65042delinsTTTGGGACAATGTAGTA
NG_016983.2:g.65026_65042delinsTTTGGGACAATGTAGTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000339077.10:c.998_1014delinsTTTGGGACAATGTAGTA MANE Select ENSP00000343273.4:p.Phe333=
ENST00000339077.9:c.998_1014delinsTTTGGGACAATGTAGTA ENSP00000343273.4:p.Phe333=
ENST00000409689.5:c.854_870delinsTTTGGGACAATGTAGTA ENSP00000386263.1:p.Phe285=
ENST00000521082.5:c.*1006_*1022delinsTTTGGGACAATGTAGTA ENSP00000430351.1:n.*1006_*1022delinsTTTGGGACAATGTAGTA
NM_001031710.2:c.998_1014delinsTTTGGGACAATGTAGTA NP_001026880.2:p.Phe333=
NM_018846.4:c.854_870delinsTTTGGGACAATGTAGTA NP_061334.4:p.Phe285=
NR_033328.1:n.1422_1438delinsTTTGGGACAATGTAGTA
XM_006715753.1:c.1037_1053delinsTTTGGGACAATGTAGTA XP_006715816.1:p.Phe346=
XM_006715754.1:c.971_987delinsTTTGGGACAATGTAGTA XP_006715817.1:p.Phe324=
XM_006715755.1:c.971_987delinsTTTGGGACAATGTAGTA XP_006715818.1:p.Phe324=
XM_006715756.1:c.893_909delinsTTTGGGACAATGTAGTA XP_006715819.1:p.Phe298=
XM_006715753.3:c.1037_1053delinsTTTGGGACAATGTAGTA XP_006715816.1:p.Phe346=
XM_006715754.3:c.971_987delinsTTTGGGACAATGTAGTA XP_006715817.1:p.Phe324=
XM_006715755.3:c.971_987delinsTTTGGGACAATGTAGTA XP_006715818.1:p.Phe324=
XM_006715756.3:c.893_909delinsTTTGGGACAATGTAGTA XP_006715819.1:p.Phe298=
XM_017012439.2:c.932_948delinsTTTGGGACAATGTAGTA XP_016867928.1:p.Phe311=
NM_001031710.3:c.998_1014delinsTTTGGGACAATGTAGTA MANE Select NP_001026880.2:p.Phe333=
NM_018846.5:c.854_870delinsTTTGGGACAATGTAGTA NP_061334.4:p.Phe285=
NR_033328.2:n.1371_1387delinsTTTGGGACAATGTAGTA