Canonical Allele Identifier: CA366981119
Gene: KLHL7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.23165711C>A , CM000669.2:g.23165711C>A GRCh38
NC_000007.13:g.23205330C>A , CM000669.1:g.23205330C>A GRCh37
NC_000007.12:g.23171855C>A NCBI36
NG_016983.1:g.64978C>A
NG_016983.2:g.64978C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000339077.10:c.950C>A MANE Select ENSP00000343273.4:p.Thr317Lys
ENST00000339077.9:c.950C>A ENSP00000343273.4:p.Thr317Lys
ENST00000409689.5:c.806C>A ENSP00000386263.1:p.Thr269Lys
ENST00000521082.5:c.*958C>A ENSP00000430351.1:n.*958C>A
NM_001031710.2:c.950C>A NP_001026880.2:p.Thr317Lys
NM_018846.4:c.806C>A NP_061334.4:p.Thr269Lys
NR_033328.1:n.1374C>A
XM_006715753.1:c.989C>A XP_006715816.1:p.Thr330Lys
XM_006715754.1:c.923C>A XP_006715817.1:p.Thr308Lys
XM_006715755.1:c.923C>A XP_006715818.1:p.Thr308Lys
XM_006715756.1:c.845C>A XP_006715819.1:p.Thr282Lys
XM_006715753.3:c.989C>A XP_006715816.1:p.Thr330Lys
XM_006715754.3:c.923C>A XP_006715817.1:p.Thr308Lys
XM_006715755.3:c.923C>A XP_006715818.1:p.Thr308Lys
XM_006715756.3:c.845C>A XP_006715819.1:p.Thr282Lys
XM_017012439.2:c.884C>A XP_016867928.1:p.Thr295Lys
NM_001031710.3:c.950C>A MANE Select NP_001026880.2:p.Thr317Lys
NM_018846.5:c.806C>A NP_061334.4:p.Thr269Lys
NR_033328.2:n.1323C>A