Canonical Allele Identifier: CA366981572
Gene: KLHL7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.23165909A>C , CM000669.2:g.23165909A>C GRCh38
NC_000007.13:g.23205528A>C , CM000669.1:g.23205528A>C GRCh37
NC_000007.12:g.23172053A>C NCBI36
NG_016983.1:g.65176A>C
NG_016983.2:g.65176A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000339077.10:c.1148A>C MANE Select ENSP00000343273.4:p.Lys383Thr
ENST00000339077.9:c.1148A>C ENSP00000343273.4:p.Lys383Thr
ENST00000409689.5:c.1004A>C ENSP00000386263.1:p.Lys335Thr
ENST00000469576.1:n.35A>C
ENST00000521082.5:c.*1156A>C ENSP00000430351.1:n.*1156A>C
NM_001031710.2:c.1148A>C NP_001026880.2:p.Lys383Thr
NM_018846.4:c.1004A>C NP_061334.4:p.Lys335Thr
NR_033328.1:n.1572A>C
XM_006715753.1:c.1187A>C XP_006715816.1:p.Lys396Thr
XM_006715754.1:c.1121A>C XP_006715817.1:p.Lys374Thr
XM_006715755.1:c.1121A>C XP_006715818.1:p.Lys374Thr
XM_006715756.1:c.1043A>C XP_006715819.1:p.Lys348Thr
XM_006715753.3:c.1187A>C XP_006715816.1:p.Lys396Thr
XM_006715754.3:c.1121A>C XP_006715817.1:p.Lys374Thr
XM_006715755.3:c.1121A>C XP_006715818.1:p.Lys374Thr
XM_006715756.3:c.1043A>C XP_006715819.1:p.Lys348Thr
XM_017012439.2:c.1082A>C XP_016867928.1:p.Lys361Thr
NM_001031710.3:c.1148A>C MANE Select NP_001026880.2:p.Lys383Thr
NM_018846.5:c.1004A>C NP_061334.4:p.Lys335Thr
NR_033328.2:n.1521A>C