Canonical Allele Identifier: CA2171877470

Gene: KNL1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40651472A= , CM000677.2:g.40651472A=	GRCh38
NC_000015.9:g.40943670A= , CM000677.1:g.40943670A=	GRCh37
NC_000015.8:g.38730962A=	NCBI36
NG_033114.1:g.62224A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000399668.7:c.6214A= MANE Select	ENSP00000382576.3:p.Asn2072=
ENST00000346991.9:c.6292A=	ENSP00000335463.6:p.Asn2098=
ENST00000399668.6:c.6214A=	ENSP00000382576.2:p.Asn2072=
ENST00000526913.5:c.3347A=
ENST00000532347.1:n.294A=
NM_144508.4:c.6214A=	NP_653091.3:p.Asn2072=
NM_170589.4:c.6292A=	NP_733468.3:p.Asn2098=
XM_011521816.1:c.5890A=	XP_011520118.1:p.Asn1964=
XM_011521817.1:c.6214A=	XP_011520119.1:p.Asn2072=
XM_017022432.1:c.5890A=	XP_016877921.1:p.Asn1964=
NM_144508.5:c.6214A= MANE Select	NP_653091.3:p.Asn2072=
NM_170589.5:c.6292A=	NP_733468.3:p.Asn2098=