Canonical Allele Identifier: CA366981146

Gene: KLHL7

Linked Data

• MyVariant Identifiers: chr7:g.23205342G>C (hg19) ; chr7:g.23165723G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.23165723G>C , CM000669.2:g.23165723G>C	GRCh38
NC_000007.13:g.23205342G>C , CM000669.1:g.23205342G>C	GRCh37
NC_000007.12:g.23171867G>C	NCBI36
NG_016983.1:g.64990G>C
NG_016983.2:g.64990G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339077.10:c.962G>C MANE Select	ENSP00000343273.4:p.Cys321Ser
ENST00000339077.9:c.962G>C	ENSP00000343273.4:p.Cys321Ser
ENST00000409689.5:c.818G>C	ENSP00000386263.1:p.Cys273Ser
ENST00000521082.5:c.*970G>C	ENSP00000430351.1:n.*970G>C
NM_001031710.2:c.962G>C	NP_001026880.2:p.Cys321Ser
NM_018846.4:c.818G>C	NP_061334.4:p.Cys273Ser
NR_033328.1:n.1386G>C
XM_006715753.1:c.1001G>C	XP_006715816.1:p.Cys334Ser
XM_006715754.1:c.935G>C	XP_006715817.1:p.Cys312Ser
XM_006715755.1:c.935G>C	XP_006715818.1:p.Cys312Ser
XM_006715756.1:c.857G>C	XP_006715819.1:p.Cys286Ser
XM_006715753.3:c.1001G>C	XP_006715816.1:p.Cys334Ser
XM_006715754.3:c.935G>C	XP_006715817.1:p.Cys312Ser
XM_006715755.3:c.935G>C	XP_006715818.1:p.Cys312Ser
XM_006715756.3:c.857G>C	XP_006715819.1:p.Cys286Ser
XM_017012439.2:c.896G>C	XP_016867928.1:p.Cys299Ser
NM_001031710.3:c.962G>C MANE Select	NP_001026880.2:p.Cys321Ser
NM_018846.5:c.818G>C	NP_061334.4:p.Cys273Ser
NR_033328.2:n.1335G>C