Canonical Allele Identifier: CA391731984

Gene: KNL1

Linked Data

• MyVariant Identifiers: chr15:g.40913946A>T (hg19) ; chr15:g.40621748A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40621748A>T , CM000677.2:g.40621748A>T	GRCh38
NC_000015.9:g.40913946A>T , CM000677.1:g.40913946A>T	GRCh37
NC_000015.8:g.38701238A>T	NCBI36
NG_033114.1:g.32500A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399668.7:c.1484A>T MANE Select	ENSP00000382576.3:p.Asp495Val
ENST00000346991.9:c.1562A>T	ENSP00000335463.6:p.Asp521Val
ENST00000399668.6:c.1484A>T	ENSP00000382576.2:p.Asp495Val
ENST00000527044.5:c.1484A>T	ENSP00000432654.2:p.Asp495Val
ENST00000533001.1:n.1629A>T
ENST00000534204.1:c.116-7576A>T	ENSP00000453857.1:n.116-7576A>T
ENST00000614337.4:n.1800A>T
NM_144508.4:c.1484A>T	NP_653091.3:p.Asp495Val
NM_170589.4:c.1562A>T	NP_733468.3:p.Asp521Val
XM_011521816.1:c.1160A>T	XP_011520118.1:p.Asp387Val
XM_011521817.1:c.1484A>T	XP_011520119.1:p.Asp495Val
XM_017022432.1:c.1160A>T	XP_016877921.1:p.Asp387Val
NM_144508.5:c.1484A>T MANE Select	NP_653091.3:p.Asp495Val
NM_170589.5:c.1562A>T	NP_733468.3:p.Asp521Val