Canonical Allele Identifier: CA366981210

Gene: KLHL7

Linked Data

• MyVariant Identifiers: chr7:g.23205371T>A (hg19) ; chr7:g.23165752T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.23165752T>A , CM000669.2:g.23165752T>A	GRCh38
NC_000007.13:g.23205371T>A , CM000669.1:g.23205371T>A	GRCh37
NC_000007.12:g.23171896T>A	NCBI36
NG_016983.1:g.65019T>A
NG_016983.2:g.65019T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339077.10:c.991T>A MANE Select	ENSP00000343273.4:p.Cys331Ser
ENST00000339077.9:c.991T>A	ENSP00000343273.4:p.Cys331Ser
ENST00000409689.5:c.847T>A	ENSP00000386263.1:p.Cys283Ser
ENST00000521082.5:c.*999T>A	ENSP00000430351.1:n.*999T>A
NM_001031710.2:c.991T>A	NP_001026880.2:p.Cys331Ser
NM_018846.4:c.847T>A	NP_061334.4:p.Cys283Ser
NR_033328.1:n.1415T>A
XM_006715753.1:c.1030T>A	XP_006715816.1:p.Cys344Ser
XM_006715754.1:c.964T>A	XP_006715817.1:p.Cys322Ser
XM_006715755.1:c.964T>A	XP_006715818.1:p.Cys322Ser
XM_006715756.1:c.886T>A	XP_006715819.1:p.Cys296Ser
XM_006715753.3:c.1030T>A	XP_006715816.1:p.Cys344Ser
XM_006715754.3:c.964T>A	XP_006715817.1:p.Cys322Ser
XM_006715755.3:c.964T>A	XP_006715818.1:p.Cys322Ser
XM_006715756.3:c.886T>A	XP_006715819.1:p.Cys296Ser
XM_017012439.2:c.925T>A	XP_016867928.1:p.Cys309Ser
NM_001031710.3:c.991T>A MANE Select	NP_001026880.2:p.Cys331Ser
NM_018846.5:c.847T>A	NP_061334.4:p.Cys283Ser
NR_033328.2:n.1364T>A