Canonical Allele Identifier: CA391731322

Gene: KNL1

Linked Data

• COSMIC: COSM961242 ; COSM961243
• MyVariant Identifiers: chr15:g.40913841C>A (hg19) ; chr15:g.40621643C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40621643C>A , CM000677.2:g.40621643C>A	GRCh38
NC_000015.9:g.40913841C>A , CM000677.1:g.40913841C>A	GRCh37
NC_000015.8:g.38701133C>A	NCBI36
NG_033114.1:g.32395C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000399668.7:c.1379C>A MANE Select	ENSP00000382576.3:p.Ala460Asp
ENST00000346991.9:c.1457C>A	ENSP00000335463.6:p.Ala486Asp
ENST00000399668.6:c.1379C>A	ENSP00000382576.2:p.Ala460Asp
ENST00000527044.5:c.1379C>A	ENSP00000432654.2:p.Ala460Asp
ENST00000533001.1:n.1524C>A
ENST00000534204.1:c.116-7681C>A	ENSP00000453857.1:n.116-7681C>A
ENST00000614337.4:n.1695C>A
NM_144508.4:c.1379C>A	NP_653091.3:p.Ala460Asp
NM_170589.4:c.1457C>A	NP_733468.3:p.Ala486Asp
XM_011521816.1:c.1055C>A	XP_011520118.1:p.Ala352Asp
XM_011521817.1:c.1379C>A	XP_011520119.1:p.Ala460Asp
XM_017022432.1:c.1055C>A	XP_016877921.1:p.Ala352Asp
NM_144508.5:c.1379C>A MANE Select	NP_653091.3:p.Ala460Asp
NM_170589.5:c.1457C>A	NP_733468.3:p.Ala486Asp