Canonical Allele Identifier: CA366981586
Gene: KLHL7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.23165915A>C , CM000669.2:g.23165915A>C GRCh38
NC_000007.13:g.23205534A>C , CM000669.1:g.23205534A>C GRCh37
NC_000007.12:g.23172059A>C NCBI36
NG_016983.1:g.65182A>C
NG_016983.2:g.65182A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000339077.10:c.1154A>C MANE Select ENSP00000343273.4:p.Tyr385Ser
ENST00000339077.9:c.1154A>C ENSP00000343273.4:p.Tyr385Ser
ENST00000409689.5:c.1010A>C ENSP00000386263.1:p.Tyr337Ser
ENST00000469576.1:n.41A>C
ENST00000521082.5:c.*1162A>C ENSP00000430351.1:n.*1162A>C
NM_001031710.2:c.1154A>C NP_001026880.2:p.Tyr385Ser
NM_018846.4:c.1010A>C NP_061334.4:p.Tyr337Ser
NR_033328.1:n.1578A>C
XM_006715753.1:c.1193A>C XP_006715816.1:p.Tyr398Ser
XM_006715754.1:c.1127A>C XP_006715817.1:p.Tyr376Ser
XM_006715755.1:c.1127A>C XP_006715818.1:p.Tyr376Ser
XM_006715756.1:c.1049A>C XP_006715819.1:p.Tyr350Ser
XM_006715753.3:c.1193A>C XP_006715816.1:p.Tyr398Ser
XM_006715754.3:c.1127A>C XP_006715817.1:p.Tyr376Ser
XM_006715755.3:c.1127A>C XP_006715818.1:p.Tyr376Ser
XM_006715756.3:c.1049A>C XP_006715819.1:p.Tyr350Ser
XM_017012439.2:c.1088A>C XP_016867928.1:p.Tyr363Ser
NM_001031710.3:c.1154A>C MANE Select NP_001026880.2:p.Tyr385Ser
NM_018846.5:c.1010A>C NP_061334.4:p.Tyr337Ser
NR_033328.2:n.1527A>C