Canonical Allele Identifier: CA2171863686

Gene: KNL1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40621789G= , CM000677.2:g.40621789G=	GRCh38
NC_000015.9:g.40913987G= , CM000677.1:g.40913987G=	GRCh37
NC_000015.8:g.38701279G=	NCBI36
NG_033114.1:g.32541G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399668.7:c.1525G= MANE Select	ENSP00000382576.3:p.Ala509=
ENST00000346991.9:c.1603G=	ENSP00000335463.6:p.Ala535=
ENST00000399668.6:c.1525G=	ENSP00000382576.2:p.Ala509=
ENST00000527044.5:c.1525G=	ENSP00000432654.2:p.Ala509=
ENST00000533001.1:n.1670G=
ENST00000534204.1:c.116-7535G=	ENSP00000453857.1:n.116-7535G=
ENST00000614337.4:n.1841G=
NM_144508.4:c.1525G=	NP_653091.3:p.Ala509=
NM_170589.4:c.1603G=	NP_733468.3:p.Ala535=
XM_011521816.1:c.1201G=	XP_011520118.1:p.Ala401=
XM_011521817.1:c.1525G=	XP_011520119.1:p.Ala509=
XM_017022432.1:c.1201G=	XP_016877921.1:p.Ala401=
NM_144508.5:c.1525G= MANE Select	NP_653091.3:p.Ala509=
NM_170589.5:c.1603G=	NP_733468.3:p.Ala535=