Canonical Allele Identifier: CA2171877473

Gene: KNL1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40651475C= , CM000677.2:g.40651475C=	GRCh38
NC_000015.9:g.40943673C= , CM000677.1:g.40943673C=	GRCh37
NC_000015.8:g.38730965C=	NCBI36
NG_033114.1:g.62227C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399668.7:c.6217C= MANE Select	ENSP00000382576.3:p.Leu2073=
ENST00000346991.9:c.6295C=	ENSP00000335463.6:p.Leu2099=
ENST00000399668.6:c.6217C=	ENSP00000382576.2:p.Leu2073=
ENST00000526913.5:c.3350C=
ENST00000532347.1:n.297C=
NM_144508.4:c.6217C=	NP_653091.3:p.Leu2073=
NM_170589.4:c.6295C=	NP_733468.3:p.Leu2099=
XM_011521816.1:c.5893C=	XP_011520118.1:p.Leu1965=
XM_011521817.1:c.6217C=	XP_011520119.1:p.Leu2073=
XM_017022432.1:c.5893C=	XP_016877921.1:p.Leu1965=
NM_144508.5:c.6217C= MANE Select	NP_653091.3:p.Leu2073=
NM_170589.5:c.6295C=	NP_733468.3:p.Leu2099=