Canonical Allele Identifier: CA489773029

Gene: KNL1

Linked Data

• MyVariant Identifiers: chr15:g.40943765G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40651567G>A , CM000677.2:g.40651567G>A	GRCh38
NC_000015.9:g.40943765G>A , CM000677.1:g.40943765G>A	GRCh37
NC_000015.8:g.38731057G>A	NCBI36
NG_033114.1:g.62319G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399668.7:c.6309G>A MANE Select	ENSP00000382576.3:p.Gln2103=
ENST00000346991.9:c.6387G>A	ENSP00000335463.6:p.Gln2129=
ENST00000399668.6:c.6309G>A	ENSP00000382576.2:p.Gln2103=
ENST00000526913.5:c.3442G>A
ENST00000532347.1:n.389G>A
NM_144508.4:c.6309G>A	NP_653091.3:p.Gln2103=
NM_170589.4:c.6387G>A	NP_733468.3:p.Gln2129=
XM_011521816.1:c.5985G>A	XP_011520118.1:p.Gln1995=
XM_011521817.1:c.6309G>A	XP_011520119.1:p.Gln2103=
XM_017022432.1:c.5985G>A	XP_016877921.1:p.Gln1995=
NM_144508.5:c.6309G>A MANE Select	NP_653091.3:p.Gln2103=
NM_170589.5:c.6387G>A	NP_733468.3:p.Gln2129=