Canonical Allele Identifier: CA919537502

Gene: KNL1

Linked Data

• dbSNP Id: rs1567007594
• gnomAD v4: 15-40621787-TAGC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40621791_40621793del , CM000677.2:g.40621791_40621793del	GRCh38
NC_000015.9:g.40913989_40913991del , CM000677.1:g.40913989_40913991del	GRCh37
NC_000015.8:g.38701281_38701283del	NCBI36
NG_033114.1:g.32543_32545del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399668.7:c.1527_1529del MANE Select	ENSP00000382576.3:p.Ala510del
ENST00000346991.9:c.1605_1607del	ENSP00000335463.6:p.Ala536del
ENST00000399668.6:c.1527_1529del	ENSP00000382576.2:p.Ala510del
ENST00000527044.5:c.1527_1529del	ENSP00000432654.2:p.Ala510del
ENST00000533001.1:n.1672_1674del
ENST00000534204.1:c.116-7533_116-7531del	ENSP00000453857.1:n.116-7533_116-7531del
ENST00000614337.4:n.1843_1845del
NM_144508.4:c.1527_1529del	NP_653091.3:p.Ala510del
NM_170589.4:c.1605_1607del	NP_733468.3:p.Ala536del
XM_011521816.1:c.1203_1205del	XP_011520118.1:p.Ala402del
XM_011521817.1:c.1527_1529del	XP_011520119.1:p.Ala510del
XM_017022432.1:c.1203_1205del	XP_016877921.1:p.Ala402del
NM_144508.5:c.1527_1529del MANE Select	NP_653091.3:p.Ala510del
NM_170589.5:c.1605_1607del	NP_733468.3:p.Ala536del