Canonical Allele Identifier: CA2682028501
Gene: KLHL7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.23167919dup , CM000669.2:g.23167919dup GRCh38
NC_000007.13:g.23207538dup , CM000669.1:g.23207538dup GRCh37
NC_000007.12:g.23174063dup NCBI36
NG_016983.1:g.67186dup
NG_016983.2:g.67186dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000339077.10:c.1261dup MANE Select ENSP00000343273.4:p.Cys421LeufsTer29
ENST00000339077.9:c.1261dup ENSP00000343273.4:p.Cys421LeufsTer29
ENST00000409689.5:c.1117dup ENSP00000386263.1:p.Cys373LeufsTer29
ENST00000469576.1:n.148dup
ENST00000521082.5:c.*1269dup ENSP00000430351.1:n.*1269dup
NM_001031710.2:c.1261dup NP_001026880.2:p.Cys421LeufsTer29
NM_018846.4:c.1117dup NP_061334.4:p.Cys373LeufsTer29
NR_033328.1:n.1685dup
XM_006715753.1:c.1300dup XP_006715816.1:p.Cys434LeufsTer29
XM_006715754.1:c.1234dup XP_006715817.1:p.Cys412LeufsTer29
XM_006715755.1:c.1234dup XP_006715818.1:p.Cys412LeufsTer29
XM_006715756.1:c.1156dup XP_006715819.1:p.Cys386LeufsTer29
XM_006715753.3:c.1300dup XP_006715816.1:p.Cys434LeufsTer29
XM_006715754.3:c.1234dup XP_006715817.1:p.Cys412LeufsTer29
XM_006715755.3:c.1234dup XP_006715818.1:p.Cys412LeufsTer29
XM_006715756.3:c.1156dup XP_006715819.1:p.Cys386LeufsTer29
XM_017012439.2:c.1195dup XP_016867928.1:p.Cys399LeufsTer29
NM_001031710.3:c.1261dup MANE Select NP_001026880.2:p.Cys421LeufsTer29
NM_018846.5:c.1117dup NP_061334.4:p.Cys373LeufsTer29
NR_033328.2:n.1634dup