Canonical Allele Identifier: CA152166

Gene: KNL1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40622633C>G , CM000677.2:g.40622633C>G	GRCh38
NC_000015.9:g.40914831C>G , CM000677.1:g.40914831C>G	GRCh37
NC_000015.8:g.38702123C>G	NCBI36
NG_033114.1:g.33385C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_144508.5:c.2369C>G MANE Select	NP_653091.3:p.Thr790Ser
ENST00000399668.7:c.2369C>G MANE Select	ENSP00000382576.3:p.Thr790Ser
NM_144508.4:c.2369C>G	NP_653091.3:p.Thr790Ser
NM_170589.4:c.2447C>G	NP_733468.3:p.Thr816Ser
NM_170589.5:c.2447C>G	NP_733468.3:p.Thr816Ser
ENST00000346991.9:c.2447C>G	ENSP00000335463.6:p.Thr816Ser
ENST00000399668.6:c.2369C>G	ENSP00000382576.2:p.Thr790Ser
ENST00000527044.5:c.2369C>G	ENSP00000432654.2:p.Thr790Ser
ENST00000533001.1:n.2514C>G
ENST00000534204.1:c.116-6691C>G	ENSP00000453857.1:n.116-6691C>G
ENST00000614337.4:n.2685C>G
XM_011521816.1:c.2045C>G	XP_011520118.1:p.Thr682Ser
XM_011521817.1:c.2369C>G	XP_011520119.1:p.Thr790Ser
XM_017022432.1:c.2045C>G	XP_016877921.1:p.Thr682Ser