Canonical Allele Identifier: CA453994436

Gene: KLHL7

Linked Data

• MyVariant Identifiers: chr7:g.23207456A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.23167837A>G , CM000669.2:g.23167837A>G	GRCh38
NC_000007.13:g.23207456A>G , CM000669.1:g.23207456A>G	GRCh37
NC_000007.12:g.23173981A>G	NCBI36
NG_016983.1:g.67104A>G
NG_016983.2:g.67104A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339077.10:c.1179A>G MANE Select	ENSP00000343273.4:p.Gly393=
ENST00000339077.9:c.1179A>G	ENSP00000343273.4:p.Gly393=
ENST00000409689.5:c.1035A>G	ENSP00000386263.1:p.Gly345=
ENST00000469576.1:n.66A>G
ENST00000521082.5:c.*1187A>G	ENSP00000430351.1:n.*1187A>G
NM_001031710.2:c.1179A>G	NP_001026880.2:p.Gly393=
NM_018846.4:c.1035A>G	NP_061334.4:p.Gly345=
NR_033328.1:n.1603A>G
XM_006715753.1:c.1218A>G	XP_006715816.1:p.Gly406=
XM_006715754.1:c.1152A>G	XP_006715817.1:p.Gly384=
XM_006715755.1:c.1152A>G	XP_006715818.1:p.Gly384=
XM_006715756.1:c.1074A>G	XP_006715819.1:p.Gly358=
XM_006715753.3:c.1218A>G	XP_006715816.1:p.Gly406=
XM_006715754.3:c.1152A>G	XP_006715817.1:p.Gly384=
XM_006715755.3:c.1152A>G	XP_006715818.1:p.Gly384=
XM_006715756.3:c.1074A>G	XP_006715819.1:p.Gly358=
XM_017012439.2:c.1113A>G	XP_016867928.1:p.Gly371=
NM_001031710.3:c.1179A>G MANE Select	NP_001026880.2:p.Gly393=
NM_018846.5:c.1035A>G	NP_061334.4:p.Gly345=
NR_033328.2:n.1552A>G