Canonical Allele Identifier: CA391732665

Gene: KNL1

Linked Data

• MyVariant Identifiers: chr15:g.40914039C>A (hg19) ; chr15:g.40621841C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40621841C>A , CM000677.2:g.40621841C>A	GRCh38
NC_000015.9:g.40914039C>A , CM000677.1:g.40914039C>A	GRCh37
NC_000015.8:g.38701331C>A	NCBI36
NG_033114.1:g.32593C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399668.7:c.1577C>A MANE Select	ENSP00000382576.3:p.Thr526Lys
ENST00000346991.9:c.1655C>A	ENSP00000335463.6:p.Thr552Lys
ENST00000399668.6:c.1577C>A	ENSP00000382576.2:p.Thr526Lys
ENST00000527044.5:c.1577C>A	ENSP00000432654.2:p.Thr526Lys
ENST00000533001.1:n.1722C>A
ENST00000534204.1:c.116-7483C>A	ENSP00000453857.1:n.116-7483C>A
ENST00000614337.4:n.1893C>A
NM_144508.4:c.1577C>A	NP_653091.3:p.Thr526Lys
NM_170589.4:c.1655C>A	NP_733468.3:p.Thr552Lys
XM_011521816.1:c.1253C>A	XP_011520118.1:p.Thr418Lys
XM_011521817.1:c.1577C>A	XP_011520119.1:p.Thr526Lys
XM_017022432.1:c.1253C>A	XP_016877921.1:p.Thr418Lys
NM_144508.5:c.1577C>A MANE Select	NP_653091.3:p.Thr526Lys
NM_170589.5:c.1655C>A	NP_733468.3:p.Thr552Lys