Canonical Allele Identifier: CA391773583

Gene: KNL1

Linked Data

• gnomAD v4: 15-40651565-C-A
• MyVariant Identifiers: chr15:g.40943763C>A (hg19) ; chr15:g.40651565C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40651565C>A , CM000677.2:g.40651565C>A	GRCh38
NC_000015.9:g.40943763C>A , CM000677.1:g.40943763C>A	GRCh37
NC_000015.8:g.38731055C>A	NCBI36
NG_033114.1:g.62317C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399668.7:c.6307C>A MANE Select	ENSP00000382576.3:p.Gln2103Lys
ENST00000346991.9:c.6385C>A	ENSP00000335463.6:p.Gln2129Lys
ENST00000399668.6:c.6307C>A	ENSP00000382576.2:p.Gln2103Lys
ENST00000526913.5:c.3440C>A
ENST00000532347.1:n.387C>A
NM_144508.4:c.6307C>A	NP_653091.3:p.Gln2103Lys
NM_170589.4:c.6385C>A	NP_733468.3:p.Gln2129Lys
XM_011521816.1:c.5983C>A	XP_011520118.1:p.Gln1995Lys
XM_011521817.1:c.6307C>A	XP_011520119.1:p.Gln2103Lys
XM_017022432.1:c.5983C>A	XP_016877921.1:p.Gln1995Lys
NM_144508.5:c.6307C>A MANE Select	NP_653091.3:p.Gln2103Lys
NM_170589.5:c.6385C>A	NP_733468.3:p.Gln2129Lys