Canonical Allele Identifier: CA268840204

Gene: KNL1

Linked Data

• dbSNP Id: rs922347772
• gnomAD v2: 15-40943790-ATTTG-A
• gnomAD v3: 15-40651592-ATTTG-A
• gnomAD v4: 15-40651592-ATTTG-A
• MyVariant Identifiers: chr15:g.40943791_40943794del (hg19) ; chr15:g.40651593_40651596del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40651598_40651601del , CM000677.2:g.40651598_40651601del	GRCh38
NC_000015.9:g.40943796_40943799del , CM000677.1:g.40943796_40943799del	GRCh37
NC_000015.8:g.38731088_38731091del	NCBI36
NG_033114.1:g.62350_62353del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399668.7:c.6314+26_6314+29del MANE Select	ENSP00000382576.3:n.6314+26_6314+29del
ENST00000346991.9:c.6392+26_6392+29del	ENSP00000335463.6:n.6392+26_6392+29del
ENST00000399668.6:c.6314+26_6314+29del	ENSP00000382576.2:n.6314+26_6314+29del
ENST00000526913.5:c.3447+26_3447+29del
ENST00000532347.1:n.394+26_394+29del
NM_144508.4:c.6314+26_6314+29del	NP_653091.3:n.6314+26_6314+29del
NM_170589.4:c.6392+26_6392+29del	NP_733468.3:n.6392+26_6392+29del
XM_011521816.1:c.5990+26_5990+29del	XP_011520118.1:n.5990+26_5990+29del
XM_011521817.1:c.6314+26_6314+29del	XP_011520119.1:n.6314+26_6314+29del
XM_017022432.1:c.5990+26_5990+29del	XP_016877921.1:n.5990+26_5990+29del
NM_144508.5:c.6314+26_6314+29del MANE Select	NP_653091.3:n.6314+26_6314+29del
NM_170589.5:c.6392+26_6392+29del	NP_733468.3:n.6392+26_6392+29del