Canonical Allele Identifier: CA366981134

Gene: KLHL7

Linked Data

• MyVariant Identifiers: chr7:g.23205336T>C (hg19) ; chr7:g.23165717T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.23165717T>C , CM000669.2:g.23165717T>C	GRCh38
NC_000007.13:g.23205336T>C , CM000669.1:g.23205336T>C	GRCh37
NC_000007.12:g.23171861T>C	NCBI36
NG_016983.1:g.64984T>C
NG_016983.2:g.64984T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339077.10:c.956T>C MANE Select	ENSP00000343273.4:p.Ile319Thr
ENST00000339077.9:c.956T>C	ENSP00000343273.4:p.Ile319Thr
ENST00000409689.5:c.812T>C	ENSP00000386263.1:p.Ile271Thr
ENST00000521082.5:c.*964T>C	ENSP00000430351.1:n.*964T>C
NM_001031710.2:c.956T>C	NP_001026880.2:p.Ile319Thr
NM_018846.4:c.812T>C	NP_061334.4:p.Ile271Thr
NR_033328.1:n.1380T>C
XM_006715753.1:c.995T>C	XP_006715816.1:p.Ile332Thr
XM_006715754.1:c.929T>C	XP_006715817.1:p.Ile310Thr
XM_006715755.1:c.929T>C	XP_006715818.1:p.Ile310Thr
XM_006715756.1:c.851T>C	XP_006715819.1:p.Ile284Thr
XM_006715753.3:c.995T>C	XP_006715816.1:p.Ile332Thr
XM_006715754.3:c.929T>C	XP_006715817.1:p.Ile310Thr
XM_006715755.3:c.929T>C	XP_006715818.1:p.Ile310Thr
XM_006715756.3:c.851T>C	XP_006715819.1:p.Ile284Thr
XM_017012439.2:c.890T>C	XP_016867928.1:p.Ile297Thr
NM_001031710.3:c.956T>C MANE Select	NP_001026880.2:p.Ile319Thr
NM_018846.5:c.812T>C	NP_061334.4:p.Ile271Thr
NR_033328.2:n.1329T>C