Canonical Allele Identifier: CA2171863634

Gene: KNL1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40621667C= , CM000677.2:g.40621667C=	GRCh38
NC_000015.9:g.40913865C= , CM000677.1:g.40913865C=	GRCh37
NC_000015.8:g.38701157C=	NCBI36
NG_033114.1:g.32419C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399668.7:c.1403C= MANE Select	ENSP00000382576.3:p.Ala468=
ENST00000346991.9:c.1481C=	ENSP00000335463.6:p.Ala494=
ENST00000399668.6:c.1403C=	ENSP00000382576.2:p.Ala468=
ENST00000527044.5:c.1403C=	ENSP00000432654.2:p.Ala468=
ENST00000533001.1:n.1548C=
ENST00000534204.1:c.116-7657C=	ENSP00000453857.1:n.116-7657C=
ENST00000614337.4:n.1719C=
NM_144508.4:c.1403C=	NP_653091.3:p.Ala468=
NM_170589.4:c.1481C=	NP_733468.3:p.Ala494=
XM_011521816.1:c.1079C=	XP_011520118.1:p.Ala360=
XM_011521817.1:c.1403C=	XP_011520119.1:p.Ala468=
XM_017022432.1:c.1079C=	XP_016877921.1:p.Ala360=
NM_144508.5:c.1403C= MANE Select	NP_653091.3:p.Ala468=
NM_170589.5:c.1481C=	NP_733468.3:p.Ala494=