Canonical Allele Identifier: CA2171858588

Gene: KNL1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40611392C= , CM000677.2:g.40611392C=	GRCh38
NC_000015.9:g.40903590C= , CM000677.1:g.40903590C=	GRCh37
NC_000015.8:g.38690882C=	NCBI36
NG_033114.1:g.22144C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399668.7:c.251-86C= MANE Select	ENSP00000382576.3:n.251-86C=
ENST00000346991.9:c.329-86C=	ENSP00000335463.6:n.329-86C=
ENST00000399668.6:c.251-86C=	ENSP00000382576.2:n.251-86C=
ENST00000527044.5:c.251-86C=	ENSP00000432654.2:n.251-86C=
ENST00000533001.1:n.396-86C=
ENST00000534204.1:c.115+4960C=	ENSP00000453857.1:n.115+4960C=
ENST00000614337.4:n.626-92C=
NM_144508.4:c.251-86C=	NP_653091.3:n.251-86C=
NM_170589.4:c.329-86C=	NP_733468.3:n.329-86C=
XM_011521817.1:c.251-86C=	XP_011520119.1:n.251-86C=
XM_017022432.1:c.-41+1095C=	XP_016877921.1:n.-41+1095C=
NM_144508.5:c.251-86C= MANE Select	NP_653091.3:n.251-86C=
NM_170589.5:c.329-86C=	NP_733468.3:n.329-86C=