Canonical Allele Identifier: CA366981542
Gene: KLHL7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.23165895T>A , CM000669.2:g.23165895T>A GRCh38
NC_000007.13:g.23205514T>A , CM000669.1:g.23205514T>A GRCh37
NC_000007.12:g.23172039T>A NCBI36
NG_016983.1:g.65162T>A
NG_016983.2:g.65162T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000339077.10:c.1134T>A MANE Select ENSP00000343273.4:p.Cys378Ter
ENST00000339077.9:c.1134T>A ENSP00000343273.4:p.Cys378Ter
ENST00000409689.5:c.990T>A ENSP00000386263.1:p.Cys330Ter
ENST00000469576.1:n.21T>A
ENST00000521082.5:c.*1142T>A ENSP00000430351.1:n.*1142T>A
NM_001031710.2:c.1134T>A NP_001026880.2:p.Cys378Ter
NM_018846.4:c.990T>A NP_061334.4:p.Cys330Ter
NR_033328.1:n.1558T>A
XM_006715753.1:c.1173T>A XP_006715816.1:p.Cys391Ter
XM_006715754.1:c.1107T>A XP_006715817.1:p.Cys369Ter
XM_006715755.1:c.1107T>A XP_006715818.1:p.Cys369Ter
XM_006715756.1:c.1029T>A XP_006715819.1:p.Cys343Ter
XM_006715753.3:c.1173T>A XP_006715816.1:p.Cys391Ter
XM_006715754.3:c.1107T>A XP_006715817.1:p.Cys369Ter
XM_006715755.3:c.1107T>A XP_006715818.1:p.Cys369Ter
XM_006715756.3:c.1029T>A XP_006715819.1:p.Cys343Ter
XM_017012439.2:c.1068T>A XP_016867928.1:p.Cys356Ter
NM_001031710.3:c.1134T>A MANE Select NP_001026880.2:p.Cys378Ter
NM_018846.5:c.990T>A NP_061334.4:p.Cys330Ter
NR_033328.2:n.1507T>A