Canonical Allele Identifier: CA2171863623

Gene: KNL1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40621642G= , CM000677.2:g.40621642G=	GRCh38
NC_000015.9:g.40913840G= , CM000677.1:g.40913840G=	GRCh37
NC_000015.8:g.38701132G=	NCBI36
NG_033114.1:g.32394G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000399668.7:c.1378G= MANE Select	ENSP00000382576.3:p.Ala460=
ENST00000346991.9:c.1456G=	ENSP00000335463.6:p.Ala486=
ENST00000399668.6:c.1378G=	ENSP00000382576.2:p.Ala460=
ENST00000527044.5:c.1378G=	ENSP00000432654.2:p.Ala460=
ENST00000533001.1:n.1523G=
ENST00000534204.1:c.116-7682G=	ENSP00000453857.1:n.116-7682G=
ENST00000614337.4:n.1694G=
NM_144508.4:c.1378G=	NP_653091.3:p.Ala460=
NM_170589.4:c.1456G=	NP_733468.3:p.Ala486=
XM_011521816.1:c.1054G=	XP_011520118.1:p.Ala352=
XM_011521817.1:c.1378G=	XP_011520119.1:p.Ala460=
XM_017022432.1:c.1054G=	XP_016877921.1:p.Ala352=
NM_144508.5:c.1378G= MANE Select	NP_653091.3:p.Ala460=
NM_170589.5:c.1456G=	NP_733468.3:p.Ala486=