Canonical Allele Identifier: CA1694330816

Gene: KLHL7

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.23165918C= , CM000669.2:g.23165918C=	GRCh38
NC_000007.13:g.23205537C= , CM000669.1:g.23205537C=	GRCh37
NC_000007.12:g.23172062C=	NCBI36
NG_016983.1:g.65185C=
NG_016983.2:g.65185C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339077.10:c.1157C= MANE Select	ENSP00000343273.4:p.Thr386=
ENST00000339077.9:c.1157C=	ENSP00000343273.4:p.Thr386=
ENST00000409689.5:c.1013C=	ENSP00000386263.1:p.Thr338=
ENST00000469576.1:n.44C=
ENST00000521082.5:c.*1165C=	ENSP00000430351.1:n.*1165C=
NM_001031710.2:c.1157C=	NP_001026880.2:p.Thr386=
NM_018846.4:c.1013C=	NP_061334.4:p.Thr338=
NR_033328.1:n.1581C=
XM_006715753.1:c.1196C=	XP_006715816.1:p.Thr399=
XM_006715754.1:c.1130C=	XP_006715817.1:p.Thr377=
XM_006715755.1:c.1130C=	XP_006715818.1:p.Thr377=
XM_006715756.1:c.1052C=	XP_006715819.1:p.Thr351=
XM_006715753.3:c.1196C=	XP_006715816.1:p.Thr399=
XM_006715754.3:c.1130C=	XP_006715817.1:p.Thr377=
XM_006715755.3:c.1130C=	XP_006715818.1:p.Thr377=
XM_006715756.3:c.1052C=	XP_006715819.1:p.Thr351=
XM_017012439.2:c.1091C=	XP_016867928.1:p.Thr364=
NM_001031710.3:c.1157C= MANE Select	NP_001026880.2:p.Thr386=
NM_018846.5:c.1013C=	NP_061334.4:p.Thr338=
NR_033328.2:n.1530C=