Canonical Allele Identifier: CA454140896

Gene: KLHL7

Linked Data

• MyVariant Identifiers: chr7:g.23205346C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.23165727C>T , CM000669.2:g.23165727C>T	GRCh38
NC_000007.13:g.23205346C>T , CM000669.1:g.23205346C>T	GRCh37
NC_000007.12:g.23171871C>T	NCBI36
NG_016983.1:g.64994C>T
NG_016983.2:g.64994C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339077.10:c.966C>T MANE Select	ENSP00000343273.4:p.Pro322=
ENST00000339077.9:c.966C>T	ENSP00000343273.4:p.Pro322=
ENST00000409689.5:c.822C>T	ENSP00000386263.1:p.Pro274=
ENST00000521082.5:c.*974C>T	ENSP00000430351.1:n.*974C>T
NM_001031710.2:c.966C>T	NP_001026880.2:p.Pro322=
NM_018846.4:c.822C>T	NP_061334.4:p.Pro274=
NR_033328.1:n.1390C>T
XM_006715753.1:c.1005C>T	XP_006715816.1:p.Pro335=
XM_006715754.1:c.939C>T	XP_006715817.1:p.Pro313=
XM_006715755.1:c.939C>T	XP_006715818.1:p.Pro313=
XM_006715756.1:c.861C>T	XP_006715819.1:p.Pro287=
XM_006715753.3:c.1005C>T	XP_006715816.1:p.Pro335=
XM_006715754.3:c.939C>T	XP_006715817.1:p.Pro313=
XM_006715755.3:c.939C>T	XP_006715818.1:p.Pro313=
XM_006715756.3:c.861C>T	XP_006715819.1:p.Pro287=
XM_017012439.2:c.900C>T	XP_016867928.1:p.Pro300=
NM_001031710.3:c.966C>T MANE Select	NP_001026880.2:p.Pro322=
NM_018846.5:c.822C>T	NP_061334.4:p.Pro274=
NR_033328.2:n.1339C>T