Canonical Allele Identifier: CA2171877472

Gene: KNL1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40651474T= , CM000677.2:g.40651474T=	GRCh38
NC_000015.9:g.40943672T= , CM000677.1:g.40943672T=	GRCh37
NC_000015.8:g.38730964T=	NCBI36
NG_033114.1:g.62226T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000399668.7:c.6216T= MANE Select	ENSP00000382576.3:p.Asn2072=
ENST00000346991.9:c.6294T=	ENSP00000335463.6:p.Asn2098=
ENST00000399668.6:c.6216T=	ENSP00000382576.2:p.Asn2072=
ENST00000526913.5:c.3349T=
ENST00000532347.1:n.296T=
NM_144508.4:c.6216T=	NP_653091.3:p.Asn2072=
NM_170589.4:c.6294T=	NP_733468.3:p.Asn2098=
XM_011521816.1:c.5892T=	XP_011520118.1:p.Asn1964=
XM_011521817.1:c.6216T=	XP_011520119.1:p.Asn2072=
XM_017022432.1:c.5892T=	XP_016877921.1:p.Asn1964=
NM_144508.5:c.6216T= MANE Select	NP_653091.3:p.Asn2072=
NM_170589.5:c.6294T=	NP_733468.3:p.Asn2098=