Canonical Allele Identifier: CA7482906

Gene: KNL1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40622992A>G , CM000677.2:g.40622992A>G	GRCh38
NC_000015.9:g.40915190A>G , CM000677.1:g.40915190A>G	GRCh37
NC_000015.8:g.38702482A>G	NCBI36
NG_033114.1:g.33744A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399668.7:c.2728A>G MANE Select	ENSP00000382576.3:p.Arg910Gly
ENST00000346991.9:c.2806A>G	ENSP00000335463.6:p.Arg936Gly
ENST00000399668.6:c.2728A>G	ENSP00000382576.2:p.Arg910Gly
ENST00000527044.5:c.2728A>G	ENSP00000432654.2:p.Arg910Gly
ENST00000533001.1:n.2873A>G
ENST00000534204.1:c.116-6332A>G	ENSP00000453857.1:n.116-6332A>G
ENST00000614337.4:n.3044A>G
NM_144508.4:c.2728A>G	NP_653091.3:p.Arg910Gly
NM_170589.4:c.2806A>G	NP_733468.3:p.Arg936Gly
XM_011521816.1:c.2404A>G	XP_011520118.1:p.Arg802Gly
XM_011521817.1:c.2728A>G	XP_011520119.1:p.Arg910Gly
XM_017022432.1:c.2404A>G	XP_016877921.1:p.Arg802Gly
NM_144508.5:c.2728A>G MANE Select	NP_653091.3:p.Arg910Gly
NM_170589.5:c.2806A>G	NP_733468.3:p.Arg936Gly