Canonical Allele Identifier: CA366981537

Gene: KLHL7

Linked Data

• MyVariant Identifiers: chr7:g.23205512T>C (hg19) ; chr7:g.23165893T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.23165893T>C , CM000669.2:g.23165893T>C	GRCh38
NC_000007.13:g.23205512T>C , CM000669.1:g.23205512T>C	GRCh37
NC_000007.12:g.23172037T>C	NCBI36
NG_016983.1:g.65160T>C
NG_016983.2:g.65160T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339077.10:c.1132T>C MANE Select	ENSP00000343273.4:p.Cys378Arg
ENST00000339077.9:c.1132T>C	ENSP00000343273.4:p.Cys378Arg
ENST00000409689.5:c.988T>C	ENSP00000386263.1:p.Cys330Arg
ENST00000469576.1:n.19T>C
ENST00000521082.5:c.*1140T>C	ENSP00000430351.1:n.*1140T>C
NM_001031710.2:c.1132T>C	NP_001026880.2:p.Cys378Arg
NM_018846.4:c.988T>C	NP_061334.4:p.Cys330Arg
NR_033328.1:n.1556T>C
XM_006715753.1:c.1171T>C	XP_006715816.1:p.Cys391Arg
XM_006715754.1:c.1105T>C	XP_006715817.1:p.Cys369Arg
XM_006715755.1:c.1105T>C	XP_006715818.1:p.Cys369Arg
XM_006715756.1:c.1027T>C	XP_006715819.1:p.Cys343Arg
XM_006715753.3:c.1171T>C	XP_006715816.1:p.Cys391Arg
XM_006715754.3:c.1105T>C	XP_006715817.1:p.Cys369Arg
XM_006715755.3:c.1105T>C	XP_006715818.1:p.Cys369Arg
XM_006715756.3:c.1027T>C	XP_006715819.1:p.Cys343Arg
XM_017012439.2:c.1066T>C	XP_016867928.1:p.Cys356Arg
NM_001031710.3:c.1132T>C MANE Select	NP_001026880.2:p.Cys378Arg
NM_018846.5:c.988T>C	NP_061334.4:p.Cys330Arg
NR_033328.2:n.1505T>C