Canonical Allele Identifier: CA2171877507

Gene: KNL1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40651566A= , CM000677.2:g.40651566A=	GRCh38
NC_000015.9:g.40943764A= , CM000677.1:g.40943764A=	GRCh37
NC_000015.8:g.38731056A=	NCBI36
NG_033114.1:g.62318A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399668.7:c.6308A= MANE Select	ENSP00000382576.3:p.Gln2103=
ENST00000346991.9:c.6386A=	ENSP00000335463.6:p.Gln2129=
ENST00000399668.6:c.6308A=	ENSP00000382576.2:p.Gln2103=
ENST00000526913.5:c.3441A=
ENST00000532347.1:n.388A=
NM_144508.4:c.6308A=	NP_653091.3:p.Gln2103=
NM_170589.4:c.6386A=	NP_733468.3:p.Gln2129=
XM_011521816.1:c.5984A=	XP_011520118.1:p.Gln1995=
XM_011521817.1:c.6308A=	XP_011520119.1:p.Gln2103=
XM_017022432.1:c.5984A=	XP_016877921.1:p.Gln1995=
NM_144508.5:c.6308A= MANE Select	NP_653091.3:p.Gln2103=
NM_170589.5:c.6386A=	NP_733468.3:p.Gln2129=