Canonical Allele Identifier: CA2774715121

Gene: KLHL7

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.23166024_23166025insACA , CM000669.2:g.23166024_23166025insACA	GRCh38
NC_000007.13:g.23205643_23205644insACA , CM000669.1:g.23205643_23205644insACA	GRCh37
NC_000007.12:g.23172168_23172169insACA	NCBI36
NG_016983.1:g.65291_65292insACA
NG_016983.2:g.65291_65292insACA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339077.10:c.1177+86_1177+87insACA MANE Select	ENSP00000343273.4:n.1177+86_1177+87insACA
ENST00000339077.9:c.1177+86_1177+87insACA	ENSP00000343273.4:n.1177+86_1177+87insACA
ENST00000409689.5:c.1033+86_1033+87insACA	ENSP00000386263.1:n.1033+86_1033+87insACA
ENST00000469576.1:n.64+86_64+87insACA
ENST00000521082.5:c.*1185+86_*1185+87insACA	ENSP00000430351.1:n.*1185+86_*1185+87insACA
NM_001031710.2:c.1177+86_1177+87insACA	NP_001026880.2:n.1177+86_1177+87insACA
NM_018846.4:c.1033+86_1033+87insACA	NP_061334.4:n.1033+86_1033+87insACA
NR_033328.1:n.1601+86_1601+87insACA
XM_006715753.1:c.1216+86_1216+87insACA	XP_006715816.1:n.1216+86_1216+87insACA
XM_006715754.1:c.1150+86_1150+87insACA	XP_006715817.1:n.1150+86_1150+87insACA
XM_006715755.1:c.1150+86_1150+87insACA	XP_006715818.1:n.1150+86_1150+87insACA
XM_006715756.1:c.1072+86_1072+87insACA	XP_006715819.1:n.1072+86_1072+87insACA
XM_006715753.3:c.1216+86_1216+87insACA	XP_006715816.1:n.1216+86_1216+87insACA
XM_006715754.3:c.1150+86_1150+87insACA	XP_006715817.1:n.1150+86_1150+87insACA
XM_006715755.3:c.1150+86_1150+87insACA	XP_006715818.1:n.1150+86_1150+87insACA
XM_006715756.3:c.1072+86_1072+87insACA	XP_006715819.1:n.1072+86_1072+87insACA
XM_017012439.2:c.1111+86_1111+87insACA	XP_016867928.1:n.1111+86_1111+87insACA
NM_001031710.3:c.1177+86_1177+87insACA MANE Select	NP_001026880.2:n.1177+86_1177+87insACA
NM_018846.5:c.1033+86_1033+87insACA	NP_061334.4:n.1033+86_1033+87insACA
NR_033328.2:n.1550+86_1550+87insACA