Canonical Allele Identifier: CA366981271
Gene: KLHL7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.23165776T>G , CM000669.2:g.23165776T>G GRCh38
NC_000007.13:g.23205395T>G , CM000669.1:g.23205395T>G GRCh37
NC_000007.12:g.23171920T>G NCBI36
NG_016983.1:g.65043T>G
NG_016983.2:g.65043T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000339077.10:c.1015T>G MANE Select ENSP00000343273.4:p.Tyr339Asp
ENST00000339077.9:c.1015T>G ENSP00000343273.4:p.Tyr339Asp
ENST00000409689.5:c.871T>G ENSP00000386263.1:p.Tyr291Asp
ENST00000521082.5:c.*1023T>G ENSP00000430351.1:n.*1023T>G
NM_001031710.2:c.1015T>G NP_001026880.2:p.Tyr339Asp
NM_018846.4:c.871T>G NP_061334.4:p.Tyr291Asp
NR_033328.1:n.1439T>G
XM_006715753.1:c.1054T>G XP_006715816.1:p.Tyr352Asp
XM_006715754.1:c.988T>G XP_006715817.1:p.Tyr330Asp
XM_006715755.1:c.988T>G XP_006715818.1:p.Tyr330Asp
XM_006715756.1:c.910T>G XP_006715819.1:p.Tyr304Asp
XM_006715753.3:c.1054T>G XP_006715816.1:p.Tyr352Asp
XM_006715754.3:c.988T>G XP_006715817.1:p.Tyr330Asp
XM_006715755.3:c.988T>G XP_006715818.1:p.Tyr330Asp
XM_006715756.3:c.910T>G XP_006715819.1:p.Tyr304Asp
XM_017012439.2:c.949T>G XP_016867928.1:p.Tyr317Asp
NM_001031710.3:c.1015T>G MANE Select NP_001026880.2:p.Tyr339Asp
NM_018846.5:c.871T>G NP_061334.4:p.Tyr291Asp
NR_033328.2:n.1388T>G