Canonical Allele Identifier: CA2627840525

Gene: KNL1

Linked Data

• gnomAD v4: 15-40651658-A-ATTTTTT

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40651658_40651659insTTTTTT , CM000677.2:g.40651658_40651659insTTTTTT	GRCh38
NC_000015.9:g.40943856_40943857insTTTTTT , CM000677.1:g.40943856_40943857insTTTTTT	GRCh37
NC_000015.8:g.38731148_38731149insTTTTTT	NCBI36
NG_033114.1:g.62410_62411insTTTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399668.7:c.6314+86_6314+87insTTTTTT MANE Select	ENSP00000382576.3:n.6314+86_6314+87insTTTTTT
ENST00000346991.9:c.6392+86_6392+87insTTTTTT	ENSP00000335463.6:n.6392+86_6392+87insTTTTTT
ENST00000399668.6:c.6314+86_6314+87insTTTTTT	ENSP00000382576.2:n.6314+86_6314+87insTTTTTT
ENST00000526913.5:c.3447+86_3447+87insTTTTTT
ENST00000532347.1:n.394+86_394+87insTTTTTT
NM_144508.4:c.6314+86_6314+87insTTTTTT	NP_653091.3:n.6314+86_6314+87insTTTTTT
NM_170589.4:c.6392+86_6392+87insTTTTTT	NP_733468.3:n.6392+86_6392+87insTTTTTT
XM_011521816.1:c.5990+86_5990+87insTTTTTT	XP_011520118.1:n.5990+86_5990+87insTTTTTT
XM_011521817.1:c.6314+86_6314+87insTTTTTT	XP_011520119.1:n.6314+86_6314+87insTTTTTT
XM_017022432.1:c.5990+86_5990+87insTTTTTT	XP_016877921.1:n.5990+86_5990+87insTTTTTT
NM_144508.5:c.6314+86_6314+87insTTTTTT MANE Select	NP_653091.3:n.6314+86_6314+87insTTTTTT
NM_170589.5:c.6392+86_6392+87insTTTTTT	NP_733468.3:n.6392+86_6392+87insTTTTTT