Canonical Allele Identifier: CA366981294

Gene: KLHL7

Linked Data

• MyVariant Identifiers: chr7:g.23205405G>T (hg19) ; chr7:g.23165786G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.23165786G>T , CM000669.2:g.23165786G>T	GRCh38
NC_000007.13:g.23205405G>T , CM000669.1:g.23205405G>T	GRCh37
NC_000007.12:g.23171930G>T	NCBI36
NG_016983.1:g.65053G>T
NG_016983.2:g.65053G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339077.10:c.1025G>T MANE Select	ENSP00000343273.4:p.Gly342Val
ENST00000339077.9:c.1025G>T	ENSP00000343273.4:p.Gly342Val
ENST00000409689.5:c.881G>T	ENSP00000386263.1:p.Gly294Val
ENST00000521082.5:c.*1033G>T	ENSP00000430351.1:n.*1033G>T
NM_001031710.2:c.1025G>T	NP_001026880.2:p.Gly342Val
NM_018846.4:c.881G>T	NP_061334.4:p.Gly294Val
NR_033328.1:n.1449G>T
XM_006715753.1:c.1064G>T	XP_006715816.1:p.Gly355Val
XM_006715754.1:c.998G>T	XP_006715817.1:p.Gly333Val
XM_006715755.1:c.998G>T	XP_006715818.1:p.Gly333Val
XM_006715756.1:c.920G>T	XP_006715819.1:p.Gly307Val
XM_006715753.3:c.1064G>T	XP_006715816.1:p.Gly355Val
XM_006715754.3:c.998G>T	XP_006715817.1:p.Gly333Val
XM_006715755.3:c.998G>T	XP_006715818.1:p.Gly333Val
XM_006715756.3:c.920G>T	XP_006715819.1:p.Gly307Val
XM_017012439.2:c.959G>T	XP_016867928.1:p.Gly320Val
NM_001031710.3:c.1025G>T MANE Select	NP_001026880.2:p.Gly342Val
NM_018846.5:c.881G>T	NP_061334.4:p.Gly294Val
NR_033328.2:n.1398G>T