Canonical Allele Identifier: CA391731314

Gene: KNL1

Linked Data

• MyVariant Identifiers: chr15:g.40913840G>A (hg19) ; chr15:g.40621642G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40621642G>A , CM000677.2:g.40621642G>A	GRCh38
NC_000015.9:g.40913840G>A , CM000677.1:g.40913840G>A	GRCh37
NC_000015.8:g.38701132G>A	NCBI36
NG_033114.1:g.32394G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000399668.7:c.1378G>A MANE Select	ENSP00000382576.3:p.Ala460Thr
ENST00000346991.9:c.1456G>A	ENSP00000335463.6:p.Ala486Thr
ENST00000399668.6:c.1378G>A	ENSP00000382576.2:p.Ala460Thr
ENST00000527044.5:c.1378G>A	ENSP00000432654.2:p.Ala460Thr
ENST00000533001.1:n.1523G>A
ENST00000534204.1:c.116-7682G>A	ENSP00000453857.1:n.116-7682G>A
ENST00000614337.4:n.1694G>A
NM_144508.4:c.1378G>A	NP_653091.3:p.Ala460Thr
NM_170589.4:c.1456G>A	NP_733468.3:p.Ala486Thr
XM_011521816.1:c.1054G>A	XP_011520118.1:p.Ala352Thr
XM_011521817.1:c.1378G>A	XP_011520119.1:p.Ala460Thr
XM_017022432.1:c.1054G>A	XP_016877921.1:p.Ala352Thr
NM_144508.5:c.1378G>A MANE Select	NP_653091.3:p.Ala460Thr
NM_170589.5:c.1456G>A	NP_733468.3:p.Ala486Thr