Canonical Allele Identifier: CA268823310

Gene: KNL1

Linked Data

• dbSNP Id: rs373605288
• MyVariant Identifiers: chr15:g.40913978G>A (hg19) ; chr15:g.40621780G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40621780G>A , CM000677.2:g.40621780G>A	GRCh38
NC_000015.9:g.40913978G>A , CM000677.1:g.40913978G>A	GRCh37
NC_000015.8:g.38701270G>A	NCBI36
NG_033114.1:g.32532G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399668.7:c.1516G>A MANE Select	ENSP00000382576.3:p.Val506Met
ENST00000346991.9:c.1594G>A	ENSP00000335463.6:p.Val532Met
ENST00000399668.6:c.1516G>A	ENSP00000382576.2:p.Val506Met
ENST00000527044.5:c.1516G>A	ENSP00000432654.2:p.Val506Met
ENST00000533001.1:n.1661G>A
ENST00000534204.1:c.116-7544G>A	ENSP00000453857.1:n.116-7544G>A
ENST00000614337.4:n.1832G>A
NM_144508.4:c.1516G>A	NP_653091.3:p.Val506Met
NM_170589.4:c.1594G>A	NP_733468.3:p.Val532Met
XM_011521816.1:c.1192G>A	XP_011520118.1:p.Val398Met
XM_011521817.1:c.1516G>A	XP_011520119.1:p.Val506Met
XM_017022432.1:c.1192G>A	XP_016877921.1:p.Val398Met
NM_144508.5:c.1516G>A MANE Select	NP_653091.3:p.Val506Met
NM_170589.5:c.1594G>A	NP_733468.3:p.Val532Met