Canonical Allele Identifier: CA366981285

Gene: KLHL7

Linked Data

• MyVariant Identifiers: chr7:g.23205401T>G (hg19) ; chr7:g.23165782T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.23165782T>G , CM000669.2:g.23165782T>G	GRCh38
NC_000007.13:g.23205401T>G , CM000669.1:g.23205401T>G	GRCh37
NC_000007.12:g.23171926T>G	NCBI36
NG_016983.1:g.65049T>G
NG_016983.2:g.65049T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339077.10:c.1021T>G MANE Select	ENSP00000343273.4:p.Leu341Val
ENST00000339077.9:c.1021T>G	ENSP00000343273.4:p.Leu341Val
ENST00000409689.5:c.877T>G	ENSP00000386263.1:p.Leu293Val
ENST00000521082.5:c.*1029T>G	ENSP00000430351.1:n.*1029T>G
NM_001031710.2:c.1021T>G	NP_001026880.2:p.Leu341Val
NM_018846.4:c.877T>G	NP_061334.4:p.Leu293Val
NR_033328.1:n.1445T>G
XM_006715753.1:c.1060T>G	XP_006715816.1:p.Leu354Val
XM_006715754.1:c.994T>G	XP_006715817.1:p.Leu332Val
XM_006715755.1:c.994T>G	XP_006715818.1:p.Leu332Val
XM_006715756.1:c.916T>G	XP_006715819.1:p.Leu306Val
XM_006715753.3:c.1060T>G	XP_006715816.1:p.Leu354Val
XM_006715754.3:c.994T>G	XP_006715817.1:p.Leu332Val
XM_006715755.3:c.994T>G	XP_006715818.1:p.Leu332Val
XM_006715756.3:c.916T>G	XP_006715819.1:p.Leu306Val
XM_017012439.2:c.955T>G	XP_016867928.1:p.Leu319Val
NM_001031710.3:c.1021T>G MANE Select	NP_001026880.2:p.Leu341Val
NM_018846.5:c.877T>G	NP_061334.4:p.Leu293Val
NR_033328.2:n.1394T>G