Canonical Allele Identifier: CA391721006

Gene: KNL1

Linked Data

• dbSNP Id: rs12911738
• gnomAD v4: 15-40611486-A-T
• MyVariant Identifiers: chr15:g.40903684A>T (hg19) ; chr15:g.40611486A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40611486A>T , CM000677.2:g.40611486A>T	GRCh38
NC_000015.9:g.40903684A>T , CM000677.1:g.40903684A>T	GRCh37
NC_000015.8:g.38690976A>T	NCBI36
NG_033114.1:g.22238A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000399668.7:c.259A>T MANE Select	ENSP00000382576.3:p.Thr87Ser
ENST00000346991.9:c.337A>T	ENSP00000335463.6:p.Thr113Ser
ENST00000399668.6:c.259A>T	ENSP00000382576.2:p.Thr87Ser
ENST00000527044.5:c.259A>T	ENSP00000432654.2:p.Thr87Ser
ENST00000533001.1:n.404A>T
ENST00000534204.1:c.115+5054A>T	ENSP00000453857.1:n.115+5054A>T
ENST00000614337.4:n.628A>T
NM_144508.4:c.259A>T	NP_653091.3:p.Thr87Ser
NM_170589.4:c.337A>T	NP_733468.3:p.Thr113Ser
XM_011521817.1:c.259A>T	XP_011520119.1:p.Thr87Ser
XM_017022432.1:c.-41+1189A>T	XP_016877921.1:n.-41+1189A>T
NM_144508.5:c.259A>T MANE Select	NP_653091.3:p.Thr87Ser
NM_170589.5:c.337A>T	NP_733468.3:p.Thr113Ser