Canonical Allele Identifier: CA2171877568

Gene: KNL1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40651695A= , CM000677.2:g.40651695A=	GRCh38
NC_000015.9:g.40943893A= , CM000677.1:g.40943893A=	GRCh37
NC_000015.8:g.38731185A=	NCBI36
NG_033114.1:g.62447A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399668.7:c.6314+123A= MANE Select	ENSP00000382576.3:n.6314+123A=
ENST00000346991.9:c.6392+123A=	ENSP00000335463.6:n.6392+123A=
ENST00000399668.6:c.6314+123A=	ENSP00000382576.2:n.6314+123A=
ENST00000526913.5:c.3447+123A=
ENST00000532347.1:n.394+123A=
NM_144508.4:c.6314+123A=	NP_653091.3:n.6314+123A=
NM_170589.4:c.6392+123A=	NP_733468.3:n.6392+123A=
XM_011521816.1:c.5990+123A=	XP_011520118.1:n.5990+123A=
XM_011521817.1:c.6314+123A=	XP_011520119.1:n.6314+123A=
XM_017022432.1:c.5990+123A=	XP_016877921.1:n.5990+123A=
NM_144508.5:c.6314+123A= MANE Select	NP_653091.3:n.6314+123A=
NM_170589.5:c.6392+123A=	NP_733468.3:n.6392+123A=