Canonical Allele Identifier: CA2627836322

Gene: KNL1

Linked Data

• gnomAD v4: 15-40611387-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40611387A>G , CM000677.2:g.40611387A>G	GRCh38
NC_000015.9:g.40903585A>G , CM000677.1:g.40903585A>G	GRCh37
NC_000015.8:g.38690877A>G	NCBI36
NG_033114.1:g.22139A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000399668.7:c.251-91A>G MANE Select	ENSP00000382576.3:n.251-91A>G
ENST00000346991.9:c.329-91A>G	ENSP00000335463.6:n.329-91A>G
ENST00000399668.6:c.251-91A>G	ENSP00000382576.2:n.251-91A>G
ENST00000527044.5:c.251-91A>G	ENSP00000432654.2:n.251-91A>G
ENST00000533001.1:n.396-91A>G
ENST00000534204.1:c.115+4955A>G	ENSP00000453857.1:n.115+4955A>G
ENST00000614337.4:n.626-97A>G
NM_144508.4:c.251-91A>G	NP_653091.3:n.251-91A>G
NM_170589.4:c.329-91A>G	NP_733468.3:n.329-91A>G
XM_011521817.1:c.251-91A>G	XP_011520119.1:n.251-91A>G
XM_017022432.1:c.-41+1090A>G	XP_016877921.1:n.-41+1090A>G
NM_144508.5:c.251-91A>G MANE Select	NP_653091.3:n.251-91A>G
NM_170589.5:c.329-91A>G	NP_733468.3:n.329-91A>G