Canonical Allele Identifier: CA2627840239

Gene: KNL1

Linked Data

• gnomAD v4: 15-40651402-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40651402C>A , CM000677.2:g.40651402C>A	GRCh38
NC_000015.9:g.40943600C>A , CM000677.1:g.40943600C>A	GRCh37
NC_000015.8:g.38730892C>A	NCBI36
NG_033114.1:g.62154C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399668.7:c.6213-69C>A MANE Select	ENSP00000382576.3:n.6213-69C>A
ENST00000346991.9:c.6291-69C>A	ENSP00000335463.6:n.6291-69C>A
ENST00000399668.6:c.6213-69C>A	ENSP00000382576.2:n.6213-69C>A
ENST00000526913.5:c.3346-69C>A
ENST00000532347.1:n.293-69C>A
NM_144508.4:c.6213-69C>A	NP_653091.3:n.6213-69C>A
NM_170589.4:c.6291-69C>A	NP_733468.3:n.6291-69C>A
XM_011521816.1:c.5889-69C>A	XP_011520118.1:n.5889-69C>A
XM_011521817.1:c.6213-69C>A	XP_011520119.1:n.6213-69C>A
XM_017022432.1:c.5889-69C>A	XP_016877921.1:n.5889-69C>A
NM_144508.5:c.6213-69C>A MANE Select	NP_653091.3:n.6213-69C>A
NM_170589.5:c.6291-69C>A	NP_733468.3:n.6291-69C>A