Canonical Allele Identifier: CA1694335279

Gene: KLHL7

Linked Data

• dbSNP Id: rs1785047556

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.23167832del , CM000669.2:g.23167832del	GRCh38
NC_000007.13:g.23207451del , CM000669.1:g.23207451del	GRCh37
NC_000007.12:g.23173976del	NCBI36
NG_016983.1:g.67099del
NG_016983.2:g.67099del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339077.10:c.1178-4del MANE Select	ENSP00000343273.4:n.1178-4del
ENST00000339077.9:c.1178-4del	ENSP00000343273.4:n.1178-4del
ENST00000409689.5:c.1034-4del	ENSP00000386263.1:n.1034-4del
ENST00000469576.1:n.65-4del
ENST00000521082.5:c.*1186-4del	ENSP00000430351.1:n.*1186-4del
NM_001031710.2:c.1178-4del	NP_001026880.2:n.1178-4del
NM_018846.4:c.1034-4del	NP_061334.4:n.1034-4del
NR_033328.1:n.1602-4del
XM_006715753.1:c.1217-4del	XP_006715816.1:n.1217-4del
XM_006715754.1:c.1151-4del	XP_006715817.1:n.1151-4del
XM_006715755.1:c.1151-4del	XP_006715818.1:n.1151-4del
XM_006715756.1:c.1073-4del	XP_006715819.1:n.1073-4del
XM_006715753.3:c.1217-4del	XP_006715816.1:n.1217-4del
XM_006715754.3:c.1151-4del	XP_006715817.1:n.1151-4del
XM_006715755.3:c.1151-4del	XP_006715818.1:n.1151-4del
XM_006715756.3:c.1073-4del	XP_006715819.1:n.1073-4del
XM_017012439.2:c.1112-4del	XP_016867928.1:n.1112-4del
NM_001031710.3:c.1178-4del MANE Select	NP_001026880.2:n.1178-4del
NM_018846.5:c.1034-4del	NP_061334.4:n.1034-4del
NR_033328.2:n.1551-4del