Canonical Allele Identifier: CA366981188

Gene: KLHL7

Linked Data

• MyVariant Identifiers: chr7:g.23205360G>T (hg19) ; chr7:g.23165741G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.23165741G>T , CM000669.2:g.23165741G>T	GRCh38
NC_000007.13:g.23205360G>T , CM000669.1:g.23205360G>T	GRCh37
NC_000007.12:g.23171885G>T	NCBI36
NG_016983.1:g.65008G>T
NG_016983.2:g.65008G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339077.10:c.980G>T MANE Select	ENSP00000343273.4:p.Arg327Ile
ENST00000339077.9:c.980G>T	ENSP00000343273.4:p.Arg327Ile
ENST00000409689.5:c.836G>T	ENSP00000386263.1:p.Arg279Ile
ENST00000521082.5:c.*988G>T	ENSP00000430351.1:n.*988G>T
NM_001031710.2:c.980G>T	NP_001026880.2:p.Arg327Ile
NM_018846.4:c.836G>T	NP_061334.4:p.Arg279Ile
NR_033328.1:n.1404G>T
XM_006715753.1:c.1019G>T	XP_006715816.1:p.Arg340Ile
XM_006715754.1:c.953G>T	XP_006715817.1:p.Arg318Ile
XM_006715755.1:c.953G>T	XP_006715818.1:p.Arg318Ile
XM_006715756.1:c.875G>T	XP_006715819.1:p.Arg292Ile
XM_006715753.3:c.1019G>T	XP_006715816.1:p.Arg340Ile
XM_006715754.3:c.953G>T	XP_006715817.1:p.Arg318Ile
XM_006715755.3:c.953G>T	XP_006715818.1:p.Arg318Ile
XM_006715756.3:c.875G>T	XP_006715819.1:p.Arg292Ile
XM_017012439.2:c.914G>T	XP_016867928.1:p.Arg305Ile
NM_001031710.3:c.980G>T MANE Select	NP_001026880.2:p.Arg327Ile
NM_018846.5:c.836G>T	NP_061334.4:p.Arg279Ile
NR_033328.2:n.1353G>T