Canonical Allele Identifier: CA391732063

Gene: KNL1

Linked Data

• gnomAD v4: 15-40621758-T-G
• COSMIC: COSM1372676 ; COSM1372677
• MyVariant Identifiers: chr15:g.40913956T>G (hg19) ; chr15:g.40621758T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40621758T>G , CM000677.2:g.40621758T>G	GRCh38
NC_000015.9:g.40913956T>G , CM000677.1:g.40913956T>G	GRCh37
NC_000015.8:g.38701248T>G	NCBI36
NG_033114.1:g.32510T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399668.7:c.1494T>G MANE Select	ENSP00000382576.3:p.Ile498Met
ENST00000346991.9:c.1572T>G	ENSP00000335463.6:p.Ile524Met
ENST00000399668.6:c.1494T>G	ENSP00000382576.2:p.Ile498Met
ENST00000527044.5:c.1494T>G	ENSP00000432654.2:p.Ile498Met
ENST00000533001.1:n.1639T>G
ENST00000534204.1:c.116-7566T>G	ENSP00000453857.1:n.116-7566T>G
ENST00000614337.4:n.1810T>G
NM_144508.4:c.1494T>G	NP_653091.3:p.Ile498Met
NM_170589.4:c.1572T>G	NP_733468.3:p.Ile524Met
XM_011521816.1:c.1170T>G	XP_011520118.1:p.Ile390Met
XM_011521817.1:c.1494T>G	XP_011520119.1:p.Ile498Met
XM_017022432.1:c.1170T>G	XP_016877921.1:p.Ile390Met
NM_144508.5:c.1494T>G MANE Select	NP_653091.3:p.Ile498Met
NM_170589.5:c.1572T>G	NP_733468.3:p.Ile524Met