Canonical Allele Identifier: CA2171877484

Gene: KNL1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40651506C= , CM000677.2:g.40651506C=	GRCh38
NC_000015.9:g.40943704C= , CM000677.1:g.40943704C=	GRCh37
NC_000015.8:g.38730996C=	NCBI36
NG_033114.1:g.62258C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399668.7:c.6248C= MANE Select	ENSP00000382576.3:p.Thr2083=
ENST00000346991.9:c.6326C=	ENSP00000335463.6:p.Thr2109=
ENST00000399668.6:c.6248C=	ENSP00000382576.2:p.Thr2083=
ENST00000526913.5:c.3381C=
ENST00000532347.1:n.328C=
NM_144508.4:c.6248C=	NP_653091.3:p.Thr2083=
NM_170589.4:c.6326C=	NP_733468.3:p.Thr2109=
XM_011521816.1:c.5924C=	XP_011520118.1:p.Thr1975=
XM_011521817.1:c.6248C=	XP_011520119.1:p.Thr2083=
XM_017022432.1:c.5924C=	XP_016877921.1:p.Thr1975=
NM_144508.5:c.6248C= MANE Select	NP_653091.3:p.Thr2083=
NM_170589.5:c.6326C=	NP_733468.3:p.Thr2109=