Canonical Allele Identifier: CA2171877525

Gene: KNL1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40651616_40651617delinsCT , CM000677.2:g.40651616_40651617delinsCT	GRCh38
NC_000015.9:g.40943814_40943815delinsCT , CM000677.1:g.40943814_40943815delinsCT	GRCh37
NC_000015.8:g.38731106_38731107delinsCT	NCBI36
NG_033114.1:g.62368_62369delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399668.7:c.6314+44_6314+45delinsCT MANE Select	ENSP00000382576.3:n.6314+44_6314+45delinsCT
ENST00000346991.9:c.6392+44_6392+45delinsCT	ENSP00000335463.6:n.6392+44_6392+45delinsCT
ENST00000399668.6:c.6314+44_6314+45delinsCT	ENSP00000382576.2:n.6314+44_6314+45delinsCT
ENST00000526913.5:c.3447+44_3447+45delinsCT
ENST00000532347.1:n.394+44_394+45delinsCT
NM_144508.4:c.6314+44_6314+45delinsCT	NP_653091.3:n.6314+44_6314+45delinsCT
NM_170589.4:c.6392+44_6392+45delinsCT	NP_733468.3:n.6392+44_6392+45delinsCT
XM_011521816.1:c.5990+44_5990+45delinsCT	XP_011520118.1:n.5990+44_5990+45delinsCT
XM_011521817.1:c.6314+44_6314+45delinsCT	XP_011520119.1:n.6314+44_6314+45delinsCT
XM_017022432.1:c.5990+44_5990+45delinsCT	XP_016877921.1:n.5990+44_5990+45delinsCT
NM_144508.5:c.6314+44_6314+45delinsCT MANE Select	NP_653091.3:n.6314+44_6314+45delinsCT
NM_170589.5:c.6392+44_6392+45delinsCT	NP_733468.3:n.6392+44_6392+45delinsCT