Canonical Allele Identifier: CA2171863746

Gene: KNL1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40621931C= , CM000677.2:g.40621931C=	GRCh38
NC_000015.9:g.40914129C= , CM000677.1:g.40914129C=	GRCh37
NC_000015.8:g.38701421C=	NCBI36
NG_033114.1:g.32683C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399668.7:c.1667C= MANE Select	ENSP00000382576.3:p.Ser556=
ENST00000346991.9:c.1745C=	ENSP00000335463.6:p.Ser582=
ENST00000399668.6:c.1667C=	ENSP00000382576.2:p.Ser556=
ENST00000527044.5:c.1667C=	ENSP00000432654.2:p.Ser556=
ENST00000533001.1:n.1812C=
ENST00000534204.1:c.116-7393C=	ENSP00000453857.1:n.116-7393C=
ENST00000614337.4:n.1983C=
NM_144508.4:c.1667C=	NP_653091.3:p.Ser556=
NM_170589.4:c.1745C=	NP_733468.3:p.Ser582=
XM_011521816.1:c.1343C=	XP_011520118.1:p.Ser448=
XM_011521817.1:c.1667C=	XP_011520119.1:p.Ser556=
XM_017022432.1:c.1343C=	XP_016877921.1:p.Ser448=
NM_144508.5:c.1667C= MANE Select	NP_653091.3:p.Ser556=
NM_170589.5:c.1745C=	NP_733468.3:p.Ser582=