Canonical Allele Identifier: CA2171877468

Gene: KNL1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40651466T= , CM000677.2:g.40651466T=	GRCh38
NC_000015.9:g.40943664T= , CM000677.1:g.40943664T=	GRCh37
NC_000015.8:g.38730956T=	NCBI36
NG_033114.1:g.62218T=

Transcript Alleles

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