Canonical Allele Identifier: CA2171877491

Gene: KNL1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40651523T= , CM000677.2:g.40651523T=	GRCh38
NC_000015.9:g.40943721T= , CM000677.1:g.40943721T=	GRCh37
NC_000015.8:g.38731013T=	NCBI36
NG_033114.1:g.62275T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399668.7:c.6265T= MANE Select	ENSP00000382576.3:p.Phe2089=
ENST00000346991.9:c.6343T=	ENSP00000335463.6:p.Phe2115=
ENST00000399668.6:c.6265T=	ENSP00000382576.2:p.Phe2089=
ENST00000526913.5:c.3398T=
ENST00000532347.1:n.345T=
NM_144508.4:c.6265T=	NP_653091.3:p.Phe2089=
NM_170589.4:c.6343T=	NP_733468.3:p.Phe2115=
XM_011521816.1:c.5941T=	XP_011520118.1:p.Phe1981=
XM_011521817.1:c.6265T=	XP_011520119.1:p.Phe2089=
XM_017022432.1:c.5941T=	XP_016877921.1:p.Phe1981=
NM_144508.5:c.6265T= MANE Select	NP_653091.3:p.Phe2089=
NM_170589.5:c.6343T=	NP_733468.3:p.Phe2115=