Canonical Allele Identifier: CA2627840545

Gene: KNL1

Linked Data

• gnomAD v4: 15-40651669-GTT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40651673_40651674del , CM000677.2:g.40651673_40651674del	GRCh38
NC_000015.9:g.40943871_40943872del , CM000677.1:g.40943871_40943872del	GRCh37
NC_000015.8:g.38731163_38731164del	NCBI36
NG_033114.1:g.62425_62426del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399668.7:c.6314+101_6314+102del MANE Select	ENSP00000382576.3:n.6314+101_6314+102del
ENST00000346991.9:c.6392+101_6392+102del	ENSP00000335463.6:n.6392+101_6392+102del
ENST00000399668.6:c.6314+101_6314+102del	ENSP00000382576.2:n.6314+101_6314+102del
ENST00000526913.5:c.3447+101_3447+102del
ENST00000532347.1:n.394+101_394+102del
NM_144508.4:c.6314+101_6314+102del	NP_653091.3:n.6314+101_6314+102del
NM_170589.4:c.6392+101_6392+102del	NP_733468.3:n.6392+101_6392+102del
XM_011521816.1:c.5990+101_5990+102del	XP_011520118.1:n.5990+101_5990+102del
XM_011521817.1:c.6314+101_6314+102del	XP_011520119.1:n.6314+101_6314+102del
XM_017022432.1:c.5990+101_5990+102del	XP_016877921.1:n.5990+101_5990+102del
NM_144508.5:c.6314+101_6314+102del MANE Select	NP_653091.3:n.6314+101_6314+102del
NM_170589.5:c.6392+101_6392+102del	NP_733468.3:n.6392+101_6392+102del