Canonical Allele Identifier: CA366981290
Gene: KLHL7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.23165784G>T , CM000669.2:g.23165784G>T GRCh38
NC_000007.13:g.23205403G>T , CM000669.1:g.23205403G>T GRCh37
NC_000007.12:g.23171928G>T NCBI36
NG_016983.1:g.65051G>T
NG_016983.2:g.65051G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000339077.10:c.1023G>T MANE Select ENSP00000343273.4:p.Leu341Phe
ENST00000339077.9:c.1023G>T ENSP00000343273.4:p.Leu341Phe
ENST00000409689.5:c.879G>T ENSP00000386263.1:p.Leu293Phe
ENST00000521082.5:c.*1031G>T ENSP00000430351.1:n.*1031G>T
NM_001031710.2:c.1023G>T NP_001026880.2:p.Leu341Phe
NM_018846.4:c.879G>T NP_061334.4:p.Leu293Phe
NR_033328.1:n.1447G>T
XM_006715753.1:c.1062G>T XP_006715816.1:p.Leu354Phe
XM_006715754.1:c.996G>T XP_006715817.1:p.Leu332Phe
XM_006715755.1:c.996G>T XP_006715818.1:p.Leu332Phe
XM_006715756.1:c.918G>T XP_006715819.1:p.Leu306Phe
XM_006715753.3:c.1062G>T XP_006715816.1:p.Leu354Phe
XM_006715754.3:c.996G>T XP_006715817.1:p.Leu332Phe
XM_006715755.3:c.996G>T XP_006715818.1:p.Leu332Phe
XM_006715756.3:c.918G>T XP_006715819.1:p.Leu306Phe
XM_017012439.2:c.957G>T XP_016867928.1:p.Leu319Phe
NM_001031710.3:c.1023G>T MANE Select NP_001026880.2:p.Leu341Phe
NM_018846.5:c.879G>T NP_061334.4:p.Leu293Phe
NR_033328.2:n.1396G>T