Canonical Allele Identifier: CA454140928

Gene: KLHL7

Linked Data

• MyVariant Identifiers: chr7:g.23205379T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.23165760T>C , CM000669.2:g.23165760T>C	GRCh38
NC_000007.13:g.23205379T>C , CM000669.1:g.23205379T>C	GRCh37
NC_000007.12:g.23171904T>C	NCBI36
NG_016983.1:g.65027T>C
NG_016983.2:g.65027T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339077.10:c.999T>C MANE Select	ENSP00000343273.4:p.Phe333=
ENST00000339077.9:c.999T>C	ENSP00000343273.4:p.Phe333=
ENST00000409689.5:c.855T>C	ENSP00000386263.1:p.Phe285=
ENST00000521082.5:c.*1007T>C	ENSP00000430351.1:n.*1007T>C
NM_001031710.2:c.999T>C	NP_001026880.2:p.Phe333=
NM_018846.4:c.855T>C	NP_061334.4:p.Phe285=
NR_033328.1:n.1423T>C
XM_006715753.1:c.1038T>C	XP_006715816.1:p.Phe346=
XM_006715754.1:c.972T>C	XP_006715817.1:p.Phe324=
XM_006715755.1:c.972T>C	XP_006715818.1:p.Phe324=
XM_006715756.1:c.894T>C	XP_006715819.1:p.Phe298=
XM_006715753.3:c.1038T>C	XP_006715816.1:p.Phe346=
XM_006715754.3:c.972T>C	XP_006715817.1:p.Phe324=
XM_006715755.3:c.972T>C	XP_006715818.1:p.Phe324=
XM_006715756.3:c.894T>C	XP_006715819.1:p.Phe298=
XM_017012439.2:c.933T>C	XP_016867928.1:p.Phe311=
NM_001031710.3:c.999T>C MANE Select	NP_001026880.2:p.Phe333=
NM_018846.5:c.855T>C	NP_061334.4:p.Phe285=
NR_033328.2:n.1372T>C