Canonical Allele Identifier: CA1694335302
Gene: KLHL7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.23167921C= , CM000669.2:g.23167921C= GRCh38
NC_000007.13:g.23207540C= , CM000669.1:g.23207540C= GRCh37
NC_000007.12:g.23174065C= NCBI36
NG_016983.1:g.67188C=
NG_016983.2:g.67188C=

Transcript Alleles

HGVS Amino-acid change
ENST00000339077.10:c.1263C= MANE Select ENSP00000343273.4:p.Cys421=
ENST00000339077.9:c.1263C= ENSP00000343273.4:p.Cys421=
ENST00000409689.5:c.1119C= ENSP00000386263.1:p.Cys373=
ENST00000469576.1:n.150C=
ENST00000521082.5:c.*1271C= ENSP00000430351.1:n.*1271C=
NM_001031710.2:c.1263C= NP_001026880.2:p.Cys421=
NM_018846.4:c.1119C= NP_061334.4:p.Cys373=
NR_033328.1:n.1687C=
XM_006715753.1:c.1302C= XP_006715816.1:p.Cys434=
XM_006715754.1:c.1236C= XP_006715817.1:p.Cys412=
XM_006715755.1:c.1236C= XP_006715818.1:p.Cys412=
XM_006715756.1:c.1158C= XP_006715819.1:p.Cys386=
XM_006715753.3:c.1302C= XP_006715816.1:p.Cys434=
XM_006715754.3:c.1236C= XP_006715817.1:p.Cys412=
XM_006715755.3:c.1236C= XP_006715818.1:p.Cys412=
XM_006715756.3:c.1158C= XP_006715819.1:p.Cys386=
XM_017012439.2:c.1197C= XP_016867928.1:p.Cys399=
NM_001031710.3:c.1263C= MANE Select NP_001026880.2:p.Cys421=
NM_018846.5:c.1119C= NP_061334.4:p.Cys373=
NR_033328.2:n.1636C=