Canonical Allele Identifier: CA366981138

Gene: KLHL7

Linked Data

• MyVariant Identifiers: chr7:g.23205338C>G (hg19) ; chr7:g.23165719C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.23165719C>G , CM000669.2:g.23165719C>G	GRCh38
NC_000007.13:g.23205338C>G , CM000669.1:g.23205338C>G	GRCh37
NC_000007.12:g.23171863C>G	NCBI36
NG_016983.1:g.64986C>G
NG_016983.2:g.64986C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339077.10:c.958C>G MANE Select	ENSP00000343273.4:p.Arg320Gly
ENST00000339077.9:c.958C>G	ENSP00000343273.4:p.Arg320Gly
ENST00000409689.5:c.814C>G	ENSP00000386263.1:p.Arg272Gly
ENST00000521082.5:c.*966C>G	ENSP00000430351.1:n.*966C>G
NM_001031710.2:c.958C>G	NP_001026880.2:p.Arg320Gly
NM_018846.4:c.814C>G	NP_061334.4:p.Arg272Gly
NR_033328.1:n.1382C>G
XM_006715753.1:c.997C>G	XP_006715816.1:p.Arg333Gly
XM_006715754.1:c.931C>G	XP_006715817.1:p.Arg311Gly
XM_006715755.1:c.931C>G	XP_006715818.1:p.Arg311Gly
XM_006715756.1:c.853C>G	XP_006715819.1:p.Arg285Gly
XM_006715753.3:c.997C>G	XP_006715816.1:p.Arg333Gly
XM_006715754.3:c.931C>G	XP_006715817.1:p.Arg311Gly
XM_006715755.3:c.931C>G	XP_006715818.1:p.Arg311Gly
XM_006715756.3:c.853C>G	XP_006715819.1:p.Arg285Gly
XM_017012439.2:c.892C>G	XP_016867928.1:p.Arg298Gly
NM_001031710.3:c.958C>G MANE Select	NP_001026880.2:p.Arg320Gly
NM_018846.5:c.814C>G	NP_061334.4:p.Arg272Gly
NR_033328.2:n.1331C>G