Canonical Allele Identifier: CA2171863665

Gene: KNL1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40621734T= , CM000677.2:g.40621734T=	GRCh38
NC_000015.9:g.40913932T= , CM000677.1:g.40913932T=	GRCh37
NC_000015.8:g.38701224T=	NCBI36
NG_033114.1:g.32486T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399668.7:c.1470T= MANE Select	ENSP00000382576.3:p.His490=
ENST00000346991.9:c.1548T=	ENSP00000335463.6:p.His516=
ENST00000399668.6:c.1470T=	ENSP00000382576.2:p.His490=
ENST00000527044.5:c.1470T=	ENSP00000432654.2:p.His490=
ENST00000533001.1:n.1615T=
ENST00000534204.1:c.116-7590T=	ENSP00000453857.1:n.116-7590T=
ENST00000614337.4:n.1786T=
NM_144508.4:c.1470T=	NP_653091.3:p.His490=
NM_170589.4:c.1548T=	NP_733468.3:p.His516=
XM_011521816.1:c.1146T=	XP_011520118.1:p.His382=
XM_011521817.1:c.1470T=	XP_011520119.1:p.His490=
XM_017022432.1:c.1146T=	XP_016877921.1:p.His382=
NM_144508.5:c.1470T= MANE Select	NP_653091.3:p.His490=
NM_170589.5:c.1548T=	NP_733468.3:p.His516=