Canonical Allele Identifier: CA391732718

Gene: KNL1

Linked Data

• MyVariant Identifiers: chr15:g.40914048A>T (hg19) ; chr15:g.40621850A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40621850A>T , CM000677.2:g.40621850A>T	GRCh38
NC_000015.9:g.40914048A>T , CM000677.1:g.40914048A>T	GRCh37
NC_000015.8:g.38701340A>T	NCBI36
NG_033114.1:g.32602A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399668.7:c.1586A>T MANE Select	ENSP00000382576.3:p.Asp529Val
ENST00000346991.9:c.1664A>T	ENSP00000335463.6:p.Asp555Val
ENST00000399668.6:c.1586A>T	ENSP00000382576.2:p.Asp529Val
ENST00000527044.5:c.1586A>T	ENSP00000432654.2:p.Asp529Val
ENST00000533001.1:n.1731A>T
ENST00000534204.1:c.116-7474A>T	ENSP00000453857.1:n.116-7474A>T
ENST00000614337.4:n.1902A>T
NM_144508.4:c.1586A>T	NP_653091.3:p.Asp529Val
NM_170589.4:c.1664A>T	NP_733468.3:p.Asp555Val
XM_011521816.1:c.1262A>T	XP_011520118.1:p.Asp421Val
XM_011521817.1:c.1586A>T	XP_011520119.1:p.Asp529Val
XM_017022432.1:c.1262A>T	XP_016877921.1:p.Asp421Val
NM_144508.5:c.1586A>T MANE Select	NP_653091.3:p.Asp529Val
NM_170589.5:c.1664A>T	NP_733468.3:p.Asp555Val