Canonical Allele Identifier: CA2171877543

Gene: KNL1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40651644A= , CM000677.2:g.40651644A=	GRCh38
NC_000015.9:g.40943842A= , CM000677.1:g.40943842A=	GRCh37
NC_000015.8:g.38731134A=	NCBI36
NG_033114.1:g.62396A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399668.7:c.6314+72A= MANE Select	ENSP00000382576.3:n.6314+72A=
ENST00000346991.9:c.6392+72A=	ENSP00000335463.6:n.6392+72A=
ENST00000399668.6:c.6314+72A=	ENSP00000382576.2:n.6314+72A=
ENST00000526913.5:c.3447+72A=
ENST00000532347.1:n.394+72A=
NM_144508.4:c.6314+72A=	NP_653091.3:n.6314+72A=
NM_170589.4:c.6392+72A=	NP_733468.3:n.6392+72A=
XM_011521816.1:c.5990+72A=	XP_011520118.1:n.5990+72A=
XM_011521817.1:c.6314+72A=	XP_011520119.1:n.6314+72A=
XM_017022432.1:c.5990+72A=	XP_016877921.1:n.5990+72A=
NM_144508.5:c.6314+72A= MANE Select	NP_653091.3:n.6314+72A=
NM_170589.5:c.6392+72A=	NP_733468.3:n.6392+72A=