Canonical Allele Identifier: CA2171877570

Gene: KNL1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40651698_40651700delinsAAG , CM000677.2:g.40651698_40651700delinsAAG	GRCh38
NC_000015.9:g.40943896_40943898delinsAAG , CM000677.1:g.40943896_40943898delinsAAG	GRCh37
NC_000015.8:g.38731188_38731190delinsAAG	NCBI36
NG_033114.1:g.62450_62452delinsAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399668.7:c.6314+126_6314+128delinsAAG MANE Select	ENSP00000382576.3:n.6314+126_6314+128delinsAAG
ENST00000346991.9:c.6392+126_6392+128delinsAAG	ENSP00000335463.6:n.6392+126_6392+128delinsAAG
ENST00000399668.6:c.6314+126_6314+128delinsAAG	ENSP00000382576.2:n.6314+126_6314+128delinsAAG
ENST00000526913.5:c.3447+126_3447+128delinsAAG
ENST00000532347.1:n.394+126_394+128delinsAAG
NM_144508.4:c.6314+126_6314+128delinsAAG	NP_653091.3:n.6314+126_6314+128delinsAAG
NM_170589.4:c.6392+126_6392+128delinsAAG	NP_733468.3:n.6392+126_6392+128delinsAAG
XM_011521816.1:c.5990+126_5990+128delinsAAG	XP_011520118.1:n.5990+126_5990+128delinsAAG
XM_011521817.1:c.6314+126_6314+128delinsAAG	XP_011520119.1:n.6314+126_6314+128delinsAAG
XM_017022432.1:c.5990+126_5990+128delinsAAG	XP_016877921.1:n.5990+126_5990+128delinsAAG
NM_144508.5:c.6314+126_6314+128delinsAAG MANE Select	NP_653091.3:n.6314+126_6314+128delinsAAG
NM_170589.5:c.6392+126_6392+128delinsAAG	NP_733468.3:n.6392+126_6392+128delinsAAG