Canonical Allele Identifier: CA2774715069

Gene: KLHL7

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.23165977T>A , CM000669.2:g.23165977T>A	GRCh38
NC_000007.13:g.23205596T>A , CM000669.1:g.23205596T>A	GRCh37
NC_000007.12:g.23172121T>A	NCBI36
NG_016983.1:g.65244T>A
NG_016983.2:g.65244T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339077.10:c.1177+39T>A MANE Select	ENSP00000343273.4:n.1177+39T>A
ENST00000339077.9:c.1177+39T>A	ENSP00000343273.4:n.1177+39T>A
ENST00000409689.5:c.1033+39T>A	ENSP00000386263.1:n.1033+39T>A
ENST00000469576.1:n.64+39T>A
ENST00000521082.5:c.*1185+39T>A	ENSP00000430351.1:n.*1185+39T>A
NM_001031710.2:c.1177+39T>A	NP_001026880.2:n.1177+39T>A
NM_018846.4:c.1033+39T>A	NP_061334.4:n.1033+39T>A
NR_033328.1:n.1601+39T>A
XM_006715753.1:c.1216+39T>A	XP_006715816.1:n.1216+39T>A
XM_006715754.1:c.1150+39T>A	XP_006715817.1:n.1150+39T>A
XM_006715755.1:c.1150+39T>A	XP_006715818.1:n.1150+39T>A
XM_006715756.1:c.1072+39T>A	XP_006715819.1:n.1072+39T>A
XM_006715753.3:c.1216+39T>A	XP_006715816.1:n.1216+39T>A
XM_006715754.3:c.1150+39T>A	XP_006715817.1:n.1150+39T>A
XM_006715755.3:c.1150+39T>A	XP_006715818.1:n.1150+39T>A
XM_006715756.3:c.1072+39T>A	XP_006715819.1:n.1072+39T>A
XM_017012439.2:c.1111+39T>A	XP_016867928.1:n.1111+39T>A
NM_001031710.3:c.1177+39T>A MANE Select	NP_001026880.2:n.1177+39T>A
NM_018846.5:c.1033+39T>A	NP_061334.4:n.1033+39T>A
NR_033328.2:n.1550+39T>A