Canonical Allele Identifier: CA2627840558

Gene: KNL1

Linked Data

• gnomAD v4: 15-40651684-AGTGCTGTTTC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40651685_40651694del , CM000677.2:g.40651685_40651694del	GRCh38
NC_000015.9:g.40943883_40943892del , CM000677.1:g.40943883_40943892del	GRCh37
NC_000015.8:g.38731175_38731184del	NCBI36
NG_033114.1:g.62437_62446del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399668.7:c.6314+113_6314+122del MANE Select	ENSP00000382576.3:n.6314+113_6314+122del
ENST00000346991.9:c.6392+113_6392+122del	ENSP00000335463.6:n.6392+113_6392+122del
ENST00000399668.6:c.6314+113_6314+122del	ENSP00000382576.2:n.6314+113_6314+122del
ENST00000526913.5:c.3447+113_3447+122del
ENST00000532347.1:n.394+113_394+122del
NM_144508.4:c.6314+113_6314+122del	NP_653091.3:n.6314+113_6314+122del
NM_170589.4:c.6392+113_6392+122del	NP_733468.3:n.6392+113_6392+122del
XM_011521816.1:c.5990+113_5990+122del	XP_011520118.1:n.5990+113_5990+122del
XM_011521817.1:c.6314+113_6314+122del	XP_011520119.1:n.6314+113_6314+122del
XM_017022432.1:c.5990+113_5990+122del	XP_016877921.1:n.5990+113_5990+122del
NM_144508.5:c.6314+113_6314+122del MANE Select	NP_653091.3:n.6314+113_6314+122del
NM_170589.5:c.6392+113_6392+122del	NP_733468.3:n.6392+113_6392+122del