Canonical Allele Identifier: CA2171877510

Gene: KNL1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40651569T= , CM000677.2:g.40651569T=	GRCh38
NC_000015.9:g.40943767T= , CM000677.1:g.40943767T=	GRCh37
NC_000015.8:g.38731059T=	NCBI36
NG_033114.1:g.62321T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399668.7:c.6311T= MANE Select	ENSP00000382576.3:p.Leu2104=
ENST00000346991.9:c.6389T=	ENSP00000335463.6:p.Leu2130=
ENST00000399668.6:c.6311T=	ENSP00000382576.2:p.Leu2104=
ENST00000526913.5:c.3444T=
ENST00000532347.1:n.391T=
NM_144508.4:c.6311T=	NP_653091.3:p.Leu2104=
NM_170589.4:c.6389T=	NP_733468.3:p.Leu2130=
XM_011521816.1:c.5987T=	XP_011520118.1:p.Leu1996=
XM_011521817.1:c.6311T=	XP_011520119.1:p.Leu2104=
XM_017022432.1:c.5987T=	XP_016877921.1:p.Leu1996=
NM_144508.5:c.6311T= MANE Select	NP_653091.3:p.Leu2104=
NM_170589.5:c.6389T=	NP_733468.3:p.Leu2130=