Canonical Allele Identifier: CA489976837

Gene: KNL1

Linked Data

• MyVariant Identifiers: chr15:g.40913872T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40621674T>G , CM000677.2:g.40621674T>G	GRCh38
NC_000015.9:g.40913872T>G , CM000677.1:g.40913872T>G	GRCh37
NC_000015.8:g.38701164T>G	NCBI36
NG_033114.1:g.32426T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399668.7:c.1410T>G MANE Select	ENSP00000382576.3:p.Ser470=
ENST00000346991.9:c.1488T>G	ENSP00000335463.6:p.Ser496=
ENST00000399668.6:c.1410T>G	ENSP00000382576.2:p.Ser470=
ENST00000527044.5:c.1410T>G	ENSP00000432654.2:p.Ser470=
ENST00000533001.1:n.1555T>G
ENST00000534204.1:c.116-7650T>G	ENSP00000453857.1:n.116-7650T>G
ENST00000614337.4:n.1726T>G
NM_144508.4:c.1410T>G	NP_653091.3:p.Ser470=
NM_170589.4:c.1488T>G	NP_733468.3:p.Ser496=
XM_011521816.1:c.1086T>G	XP_011520118.1:p.Ser362=
XM_011521817.1:c.1410T>G	XP_011520119.1:p.Ser470=
XM_017022432.1:c.1086T>G	XP_016877921.1:p.Ser362=
NM_144508.5:c.1410T>G MANE Select	NP_653091.3:p.Ser470=
NM_170589.5:c.1488T>G	NP_733468.3:p.Ser496=