Canonical Allele Identifier: CA489976858

Gene: KNL1

Linked Data

• COSMIC: COSM1372680 ; COSM1372681
• MyVariant Identifiers: chr15:g.40914053del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40621858del , CM000677.2:g.40621858del	GRCh38
NC_000015.9:g.40914056del , CM000677.1:g.40914056del	GRCh37
NC_000015.8:g.38701348del	NCBI36
NG_033114.1:g.32610del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399668.7:c.1594del MANE Select	ENSP00000382576.3:p.Met532Ter
ENST00000346991.9:c.1672del	ENSP00000335463.6:p.Met558Ter
ENST00000399668.6:c.1594del	ENSP00000382576.2:p.Met532Ter
ENST00000527044.5:c.1594del	ENSP00000432654.2:p.Met532Ter
ENST00000533001.1:n.1739del
ENST00000534204.1:c.116-7466del	ENSP00000453857.1:n.116-7466del
ENST00000614337.4:n.1910del
NM_144508.4:c.1594del	NP_653091.3:p.Met532Ter
NM_170589.4:c.1672del	NP_733468.3:p.Met558Ter
XM_011521816.1:c.1270del	XP_011520118.1:p.Met424Ter
XM_011521817.1:c.1594del	XP_011520119.1:p.Met532Ter
XM_017022432.1:c.1270del	XP_016877921.1:p.Met424Ter
NM_144508.5:c.1594del MANE Select	NP_653091.3:p.Met532Ter
NM_170589.5:c.1672del	NP_733468.3:p.Met558Ter