Canonical Allele Identifier: CA366981238

Gene: KLHL7

Linked Data

• MyVariant Identifiers: chr7:g.23205382G>A (hg19) ; chr7:g.23165763G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.23165763G>A , CM000669.2:g.23165763G>A	GRCh38
NC_000007.13:g.23205382G>A , CM000669.1:g.23205382G>A	GRCh37
NC_000007.12:g.23171907G>A	NCBI36
NG_016983.1:g.65030G>A
NG_016983.2:g.65030G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339077.10:c.1002G>A MANE Select	ENSP00000343273.4:p.Trp334Ter
ENST00000339077.9:c.1002G>A	ENSP00000343273.4:p.Trp334Ter
ENST00000409689.5:c.858G>A	ENSP00000386263.1:p.Trp286Ter
ENST00000521082.5:c.*1010G>A	ENSP00000430351.1:n.*1010G>A
NM_001031710.2:c.1002G>A	NP_001026880.2:p.Trp334Ter
NM_018846.4:c.858G>A	NP_061334.4:p.Trp286Ter
NR_033328.1:n.1426G>A
XM_006715753.1:c.1041G>A	XP_006715816.1:p.Trp347Ter
XM_006715754.1:c.975G>A	XP_006715817.1:p.Trp325Ter
XM_006715755.1:c.975G>A	XP_006715818.1:p.Trp325Ter
XM_006715756.1:c.897G>A	XP_006715819.1:p.Trp299Ter
XM_006715753.3:c.1041G>A	XP_006715816.1:p.Trp347Ter
XM_006715754.3:c.975G>A	XP_006715817.1:p.Trp325Ter
XM_006715755.3:c.975G>A	XP_006715818.1:p.Trp325Ter
XM_006715756.3:c.897G>A	XP_006715819.1:p.Trp299Ter
XM_017012439.2:c.936G>A	XP_016867928.1:p.Trp312Ter
NM_001031710.3:c.1002G>A MANE Select	NP_001026880.2:p.Trp334Ter
NM_018846.5:c.858G>A	NP_061334.4:p.Trp286Ter
NR_033328.2:n.1375G>A