Canonical Allele Identifier: CA2627840569

Gene: KNL1

Linked Data

• gnomAD v4: 15-40651700-GAGTC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40651704_40651707del , CM000677.2:g.40651704_40651707del	GRCh38
NC_000015.9:g.40943902_40943905del , CM000677.1:g.40943902_40943905del	GRCh37
NC_000015.8:g.38731194_38731197del	NCBI36
NG_033114.1:g.62456_62459del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399668.7:c.6314+132_6314+135del MANE Select	ENSP00000382576.3:n.6314+132_6314+135del
ENST00000346991.9:c.6392+132_6392+135del	ENSP00000335463.6:n.6392+132_6392+135del
ENST00000399668.6:c.6314+132_6314+135del	ENSP00000382576.2:n.6314+132_6314+135del
ENST00000526913.5:c.3447+132_3447+135del
ENST00000532347.1:n.394+132_394+135del
NM_144508.4:c.6314+132_6314+135del	NP_653091.3:n.6314+132_6314+135del
NM_170589.4:c.6392+132_6392+135del	NP_733468.3:n.6392+132_6392+135del
XM_011521816.1:c.5990+132_5990+135del	XP_011520118.1:n.5990+132_5990+135del
XM_011521817.1:c.6314+132_6314+135del	XP_011520119.1:n.6314+132_6314+135del
XM_017022432.1:c.5990+132_5990+135del	XP_016877921.1:n.5990+132_5990+135del
NM_144508.5:c.6314+132_6314+135del MANE Select	NP_653091.3:n.6314+132_6314+135del
NM_170589.5:c.6392+132_6392+135del	NP_733468.3:n.6392+132_6392+135del