Canonical Allele Identifier: CA2774715054

Gene: KLHL7

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.23165670G>T , CM000669.2:g.23165670G>T	GRCh38
NC_000007.13:g.23205289G>T , CM000669.1:g.23205289G>T	GRCh37
NC_000007.12:g.23171814G>T	NCBI36
NG_016983.1:g.64937G>T
NG_016983.2:g.64937G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339077.10:c.937-28G>T MANE Select	ENSP00000343273.4:n.937-28G>T
ENST00000339077.9:c.937-28G>T	ENSP00000343273.4:n.937-28G>T
ENST00000409689.5:c.793-28G>T	ENSP00000386263.1:n.793-28G>T
ENST00000521082.5:c.*945-28G>T	ENSP00000430351.1:n.*945-28G>T
NM_001031710.2:c.937-28G>T	NP_001026880.2:n.937-28G>T
NM_018846.4:c.793-28G>T	NP_061334.4:n.793-28G>T
NR_033328.1:n.1361-28G>T
XM_006715753.1:c.976-28G>T	XP_006715816.1:n.976-28G>T
XM_006715754.1:c.910-28G>T	XP_006715817.1:n.910-28G>T
XM_006715755.1:c.910-28G>T	XP_006715818.1:n.910-28G>T
XM_006715756.1:c.832-28G>T	XP_006715819.1:n.832-28G>T
XM_006715753.3:c.976-28G>T	XP_006715816.1:n.976-28G>T
XM_006715754.3:c.910-28G>T	XP_006715817.1:n.910-28G>T
XM_006715755.3:c.910-28G>T	XP_006715818.1:n.910-28G>T
XM_006715756.3:c.832-28G>T	XP_006715819.1:n.832-28G>T
XM_017012439.2:c.871-28G>T	XP_016867928.1:n.871-28G>T
NM_001031710.3:c.937-28G>T MANE Select	NP_001026880.2:n.937-28G>T
NM_018846.5:c.793-28G>T	NP_061334.4:n.793-28G>T
NR_033328.2:n.1310-28G>T