Canonical Allele Identifier: CA454141291

Gene: KLHL7

Linked Data

• MyVariant Identifiers: chr7:g.23205511A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.23165892A>C , CM000669.2:g.23165892A>C	GRCh38
NC_000007.13:g.23205511A>C , CM000669.1:g.23205511A>C	GRCh37
NC_000007.12:g.23172036A>C	NCBI36
NG_016983.1:g.65159A>C
NG_016983.2:g.65159A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339077.10:c.1131A>C MANE Select	ENSP00000343273.4:p.Ala377=
ENST00000339077.9:c.1131A>C	ENSP00000343273.4:p.Ala377=
ENST00000409689.5:c.987A>C	ENSP00000386263.1:p.Ala329=
ENST00000469576.1:n.18A>C
ENST00000521082.5:c.*1139A>C	ENSP00000430351.1:n.*1139A>C
NM_001031710.2:c.1131A>C	NP_001026880.2:p.Ala377=
NM_018846.4:c.987A>C	NP_061334.4:p.Ala329=
NR_033328.1:n.1555A>C
XM_006715753.1:c.1170A>C	XP_006715816.1:p.Ala390=
XM_006715754.1:c.1104A>C	XP_006715817.1:p.Ala368=
XM_006715755.1:c.1104A>C	XP_006715818.1:p.Ala368=
XM_006715756.1:c.1026A>C	XP_006715819.1:p.Ala342=
XM_006715753.3:c.1170A>C	XP_006715816.1:p.Ala390=
XM_006715754.3:c.1104A>C	XP_006715817.1:p.Ala368=
XM_006715755.3:c.1104A>C	XP_006715818.1:p.Ala368=
XM_006715756.3:c.1026A>C	XP_006715819.1:p.Ala342=
XM_017012439.2:c.1065A>C	XP_016867928.1:p.Ala355=
NM_001031710.3:c.1131A>C MANE Select	NP_001026880.2:p.Ala377=
NM_018846.5:c.987A>C	NP_061334.4:p.Ala329=
NR_033328.2:n.1504A>C