Canonical Allele Identifier: CA454140913

Gene: KLHL7

Linked Data

• MyVariant Identifiers: chr7:g.23205361A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.23165742A>G , CM000669.2:g.23165742A>G	GRCh38
NC_000007.13:g.23205361A>G , CM000669.1:g.23205361A>G	GRCh37
NC_000007.12:g.23171886A>G	NCBI36
NG_016983.1:g.65009A>G
NG_016983.2:g.65009A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339077.10:c.981A>G MANE Select	ENSP00000343273.4:p.Arg327=
ENST00000339077.9:c.981A>G	ENSP00000343273.4:p.Arg327=
ENST00000409689.5:c.837A>G	ENSP00000386263.1:p.Arg279=
ENST00000521082.5:c.*989A>G	ENSP00000430351.1:n.*989A>G
NM_001031710.2:c.981A>G	NP_001026880.2:p.Arg327=
NM_018846.4:c.837A>G	NP_061334.4:p.Arg279=
NR_033328.1:n.1405A>G
XM_006715753.1:c.1020A>G	XP_006715816.1:p.Arg340=
XM_006715754.1:c.954A>G	XP_006715817.1:p.Arg318=
XM_006715755.1:c.954A>G	XP_006715818.1:p.Arg318=
XM_006715756.1:c.876A>G	XP_006715819.1:p.Arg292=
XM_006715753.3:c.1020A>G	XP_006715816.1:p.Arg340=
XM_006715754.3:c.954A>G	XP_006715817.1:p.Arg318=
XM_006715755.3:c.954A>G	XP_006715818.1:p.Arg318=
XM_006715756.3:c.876A>G	XP_006715819.1:p.Arg292=
XM_017012439.2:c.915A>G	XP_016867928.1:p.Arg305=
NM_001031710.3:c.981A>G MANE Select	NP_001026880.2:p.Arg327=
NM_018846.5:c.837A>G	NP_061334.4:p.Arg279=
NR_033328.2:n.1354A>G