Canonical Allele Identifier: CA489977149

Gene: KNL1

Linked Data

• MyVariant Identifiers: chr15:g.40913968T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40621770T>C , CM000677.2:g.40621770T>C	GRCh38
NC_000015.9:g.40913968T>C , CM000677.1:g.40913968T>C	GRCh37
NC_000015.8:g.38701260T>C	NCBI36
NG_033114.1:g.32522T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399668.7:c.1506T>C MANE Select	ENSP00000382576.3:p.Asp502=
ENST00000346991.9:c.1584T>C	ENSP00000335463.6:p.Asp528=
ENST00000399668.6:c.1506T>C	ENSP00000382576.2:p.Asp502=
ENST00000527044.5:c.1506T>C	ENSP00000432654.2:p.Asp502=
ENST00000533001.1:n.1651T>C
ENST00000534204.1:c.116-7554T>C	ENSP00000453857.1:n.116-7554T>C
ENST00000614337.4:n.1822T>C
NM_144508.4:c.1506T>C	NP_653091.3:p.Asp502=
NM_170589.4:c.1584T>C	NP_733468.3:p.Asp528=
XM_011521816.1:c.1182T>C	XP_011520118.1:p.Asp394=
XM_011521817.1:c.1506T>C	XP_011520119.1:p.Asp502=
XM_017022432.1:c.1182T>C	XP_016877921.1:p.Asp394=
NM_144508.5:c.1506T>C MANE Select	NP_653091.3:p.Asp502=
NM_170589.5:c.1584T>C	NP_733468.3:p.Asp528=