Canonical Allele Identifier: CA366981114

Gene: KLHL7

Linked Data

• MyVariant Identifiers: chr7:g.23205328G>C (hg19) ; chr7:g.23165709G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.23165709G>C , CM000669.2:g.23165709G>C	GRCh38
NC_000007.13:g.23205328G>C , CM000669.1:g.23205328G>C	GRCh37
NC_000007.12:g.23171853G>C	NCBI36
NG_016983.1:g.64976G>C
NG_016983.2:g.64976G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339077.10:c.948G>C MANE Select	ENSP00000343273.4:p.Trp316Cys
ENST00000339077.9:c.948G>C	ENSP00000343273.4:p.Trp316Cys
ENST00000409689.5:c.804G>C	ENSP00000386263.1:p.Trp268Cys
ENST00000521082.5:c.*956G>C	ENSP00000430351.1:n.*956G>C
NM_001031710.2:c.948G>C	NP_001026880.2:p.Trp316Cys
NM_018846.4:c.804G>C	NP_061334.4:p.Trp268Cys
NR_033328.1:n.1372G>C
XM_006715753.1:c.987G>C	XP_006715816.1:p.Trp329Cys
XM_006715754.1:c.921G>C	XP_006715817.1:p.Trp307Cys
XM_006715755.1:c.921G>C	XP_006715818.1:p.Trp307Cys
XM_006715756.1:c.843G>C	XP_006715819.1:p.Trp281Cys
XM_006715753.3:c.987G>C	XP_006715816.1:p.Trp329Cys
XM_006715754.3:c.921G>C	XP_006715817.1:p.Trp307Cys
XM_006715755.3:c.921G>C	XP_006715818.1:p.Trp307Cys
XM_006715756.3:c.843G>C	XP_006715819.1:p.Trp281Cys
XM_017012439.2:c.882G>C	XP_016867928.1:p.Trp294Cys
NM_001031710.3:c.948G>C MANE Select	NP_001026880.2:p.Trp316Cys
NM_018846.5:c.804G>C	NP_061334.4:p.Trp268Cys
NR_033328.2:n.1321G>C