Canonical Allele Identifier: CA2171858612

Gene: KNL1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40611410C= , CM000677.2:g.40611410C=	GRCh38
NC_000015.9:g.40903608C= , CM000677.1:g.40903608C=	GRCh37
NC_000015.8:g.38690900C=	NCBI36
NG_033114.1:g.22162C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399668.7:c.251-68C= MANE Select	ENSP00000382576.3:n.251-68C=
ENST00000346991.9:c.329-68C=	ENSP00000335463.6:n.329-68C=
ENST00000399668.6:c.251-68C=	ENSP00000382576.2:n.251-68C=
ENST00000527044.5:c.251-68C=	ENSP00000432654.2:n.251-68C=
ENST00000533001.1:n.396-68C=
ENST00000534204.1:c.115+4978C=	ENSP00000453857.1:n.115+4978C=
ENST00000614337.4:n.626-74C=
NM_144508.4:c.251-68C=	NP_653091.3:n.251-68C=
NM_170589.4:c.329-68C=	NP_733468.3:n.329-68C=
XM_011521817.1:c.251-68C=	XP_011520119.1:n.251-68C=
XM_017022432.1:c.-41+1113C=	XP_016877921.1:n.-41+1113C=
NM_144508.5:c.251-68C= MANE Select	NP_653091.3:n.251-68C=
NM_170589.5:c.329-68C=	NP_733468.3:n.329-68C=