Canonical Allele Identifier: CA2682028395

Gene: KLHL7

Linked Data

• gnomAD v4: 7-23166066-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.23166066G>T , CM000669.2:g.23166066G>T	GRCh38
NC_000007.13:g.23205685G>T , CM000669.1:g.23205685G>T	GRCh37
NC_000007.12:g.23172210G>T	NCBI36
NG_016983.1:g.65333G>T
NG_016983.2:g.65333G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339077.10:c.1177+128G>T MANE Select	ENSP00000343273.4:n.1177+128G>T
ENST00000339077.9:c.1177+128G>T	ENSP00000343273.4:n.1177+128G>T
ENST00000409689.5:c.1033+128G>T	ENSP00000386263.1:n.1033+128G>T
ENST00000469576.1:n.64+128G>T
ENST00000521082.5:c.*1185+128G>T	ENSP00000430351.1:n.*1185+128G>T
NM_001031710.2:c.1177+128G>T	NP_001026880.2:n.1177+128G>T
NM_018846.4:c.1033+128G>T	NP_061334.4:n.1033+128G>T
NR_033328.1:n.1601+128G>T
XM_006715753.1:c.1216+128G>T	XP_006715816.1:n.1216+128G>T
XM_006715754.1:c.1150+128G>T	XP_006715817.1:n.1150+128G>T
XM_006715755.1:c.1150+128G>T	XP_006715818.1:n.1150+128G>T
XM_006715756.1:c.1072+128G>T	XP_006715819.1:n.1072+128G>T
XM_006715753.3:c.1216+128G>T	XP_006715816.1:n.1216+128G>T
XM_006715754.3:c.1150+128G>T	XP_006715817.1:n.1150+128G>T
XM_006715755.3:c.1150+128G>T	XP_006715818.1:n.1150+128G>T
XM_006715756.3:c.1072+128G>T	XP_006715819.1:n.1072+128G>T
XM_017012439.2:c.1111+128G>T	XP_016867928.1:n.1111+128G>T
NM_001031710.3:c.1177+128G>T MANE Select	NP_001026880.2:n.1177+128G>T
NM_018846.5:c.1033+128G>T	NP_061334.4:n.1033+128G>T
NR_033328.2:n.1550+128G>T