Canonical Allele Identifier: CA2774715168

Gene: KLHL7

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.23166076_23166077insCG , CM000669.2:g.23166076_23166077insCG	GRCh38
NC_000007.13:g.23205695_23205696insCG , CM000669.1:g.23205695_23205696insCG	GRCh37
NC_000007.12:g.23172220_23172221insCG	NCBI36
NG_016983.1:g.65343_65344insCG
NG_016983.2:g.65343_65344insCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339077.10:c.1177+138_1177+139insCG MANE Select	ENSP00000343273.4:n.1177+138_1177+139insCG
ENST00000339077.9:c.1177+138_1177+139insCG	ENSP00000343273.4:n.1177+138_1177+139insCG
ENST00000409689.5:c.1033+138_1033+139insCG	ENSP00000386263.1:n.1033+138_1033+139insCG
ENST00000469576.1:n.64+138_64+139insCG
ENST00000521082.5:c.*1185+138_*1185+139insCG	ENSP00000430351.1:n.*1185+138_*1185+139insCG
NM_001031710.2:c.1177+138_1177+139insCG	NP_001026880.2:n.1177+138_1177+139insCG
NM_018846.4:c.1033+138_1033+139insCG	NP_061334.4:n.1033+138_1033+139insCG
NR_033328.1:n.1601+138_1601+139insCG
XM_006715753.1:c.1216+138_1216+139insCG	XP_006715816.1:n.1216+138_1216+139insCG
XM_006715754.1:c.1150+138_1150+139insCG	XP_006715817.1:n.1150+138_1150+139insCG
XM_006715755.1:c.1150+138_1150+139insCG	XP_006715818.1:n.1150+138_1150+139insCG
XM_006715756.1:c.1072+138_1072+139insCG	XP_006715819.1:n.1072+138_1072+139insCG
XM_006715753.3:c.1216+138_1216+139insCG	XP_006715816.1:n.1216+138_1216+139insCG
XM_006715754.3:c.1150+138_1150+139insCG	XP_006715817.1:n.1150+138_1150+139insCG
XM_006715755.3:c.1150+138_1150+139insCG	XP_006715818.1:n.1150+138_1150+139insCG
XM_006715756.3:c.1072+138_1072+139insCG	XP_006715819.1:n.1072+138_1072+139insCG
XM_017012439.2:c.1111+138_1111+139insCG	XP_016867928.1:n.1111+138_1111+139insCG
NM_001031710.3:c.1177+138_1177+139insCG MANE Select	NP_001026880.2:n.1177+138_1177+139insCG
NM_018846.5:c.1033+138_1033+139insCG	NP_061334.4:n.1033+138_1033+139insCG
NR_033328.2:n.1550+138_1550+139insCG