Canonical Allele Identifier: CA454140951

Gene: KLHL7

Linked Data

• MyVariant Identifiers: chr7:g.23205394A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.23165775A>T , CM000669.2:g.23165775A>T	GRCh38
NC_000007.13:g.23205394A>T , CM000669.1:g.23205394A>T	GRCh37
NC_000007.12:g.23171919A>T	NCBI36
NG_016983.1:g.65042A>T
NG_016983.2:g.65042A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339077.10:c.1014A>T MANE Select	ENSP00000343273.4:p.Val338=
ENST00000339077.9:c.1014A>T	ENSP00000343273.4:p.Val338=
ENST00000409689.5:c.870A>T	ENSP00000386263.1:p.Val290=
ENST00000521082.5:c.*1022A>T	ENSP00000430351.1:n.*1022A>T
NM_001031710.2:c.1014A>T	NP_001026880.2:p.Val338=
NM_018846.4:c.870A>T	NP_061334.4:p.Val290=
NR_033328.1:n.1438A>T
XM_006715753.1:c.1053A>T	XP_006715816.1:p.Val351=
XM_006715754.1:c.987A>T	XP_006715817.1:p.Val329=
XM_006715755.1:c.987A>T	XP_006715818.1:p.Val329=
XM_006715756.1:c.909A>T	XP_006715819.1:p.Val303=
XM_006715753.3:c.1053A>T	XP_006715816.1:p.Val351=
XM_006715754.3:c.987A>T	XP_006715817.1:p.Val329=
XM_006715755.3:c.987A>T	XP_006715818.1:p.Val329=
XM_006715756.3:c.909A>T	XP_006715819.1:p.Val303=
XM_017012439.2:c.948A>T	XP_016867928.1:p.Val316=
NM_001031710.3:c.1014A>T MANE Select	NP_001026880.2:p.Val338=
NM_018846.5:c.870A>T	NP_061334.4:p.Val290=
NR_033328.2:n.1387A>T