Canonical Allele Identifier: CA2171863685

Gene: KNL1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40621787_40621790delinsTAGC , CM000677.2:g.40621787_40621790delinsTAGC	GRCh38
NC_000015.9:g.40913985_40913988delinsTAGC , CM000677.1:g.40913985_40913988delinsTAGC	GRCh37
NC_000015.8:g.38701277_38701280delinsTAGC	NCBI36
NG_033114.1:g.32539_32542delinsTAGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399668.7:c.1523_1526delinsTAGC MANE Select	ENSP00000382576.3:p.Ile508=
ENST00000346991.9:c.1601_1604delinsTAGC	ENSP00000335463.6:p.Ile534=
ENST00000399668.6:c.1523_1526delinsTAGC	ENSP00000382576.2:p.Ile508=
ENST00000527044.5:c.1523_1526delinsTAGC	ENSP00000432654.2:p.Ile508=
ENST00000533001.1:n.1668_1671delinsTAGC
ENST00000534204.1:c.116-7537_116-7534delinsTAGC	ENSP00000453857.1:n.116-7537_116-7534delinsTAGC
ENST00000614337.4:n.1839_1842delinsTAGC
NM_144508.4:c.1523_1526delinsTAGC	NP_653091.3:p.Ile508=
NM_170589.4:c.1601_1604delinsTAGC	NP_733468.3:p.Ile534=
XM_011521816.1:c.1199_1202delinsTAGC	XP_011520118.1:p.Ile400=
XM_011521817.1:c.1523_1526delinsTAGC	XP_011520119.1:p.Ile508=
XM_017022432.1:c.1199_1202delinsTAGC	XP_016877921.1:p.Ile400=
NM_144508.5:c.1523_1526delinsTAGC MANE Select	NP_653091.3:p.Ile508=
NM_170589.5:c.1601_1604delinsTAGC	NP_733468.3:p.Ile534=