Canonical Allele Identifier: CA2171877447

Gene: KNL1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40651425C= , CM000677.2:g.40651425C=	GRCh38
NC_000015.9:g.40943623C= , CM000677.1:g.40943623C=	GRCh37
NC_000015.8:g.38730915C=	NCBI36
NG_033114.1:g.62177C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399668.7:c.6213-46C= MANE Select	ENSP00000382576.3:n.6213-46C=
ENST00000346991.9:c.6291-46C=	ENSP00000335463.6:n.6291-46C=
ENST00000399668.6:c.6213-46C=	ENSP00000382576.2:n.6213-46C=
ENST00000526913.5:c.3346-46C=
ENST00000532347.1:n.293-46C=
NM_144508.4:c.6213-46C=	NP_653091.3:n.6213-46C=
NM_170589.4:c.6291-46C=	NP_733468.3:n.6291-46C=
XM_011521816.1:c.5889-46C=	XP_011520118.1:n.5889-46C=
XM_011521817.1:c.6213-46C=	XP_011520119.1:n.6213-46C=
XM_017022432.1:c.5889-46C=	XP_016877921.1:n.5889-46C=
NM_144508.5:c.6213-46C= MANE Select	NP_653091.3:n.6213-46C=
NM_170589.5:c.6291-46C=	NP_733468.3:n.6291-46C=