Canonical Allele Identifier: CA489976877

Gene: KNL1

Linked Data

• dbSNP Id: rs1395490071
• gnomAD v3: 15-40621875-C-T
• gnomAD v4: 15-40621875-C-T
• MyVariant Identifiers: chr15:g.40914073C>T (hg19) ; chr15:g.40621875C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40621875C>T , CM000677.2:g.40621875C>T	GRCh38
NC_000015.9:g.40914073C>T , CM000677.1:g.40914073C>T	GRCh37
NC_000015.8:g.38701365C>T	NCBI36
NG_033114.1:g.32627C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399668.7:c.1611C>T MANE Select	ENSP00000382576.3:p.Asn537=
ENST00000346991.9:c.1689C>T	ENSP00000335463.6:p.Asn563=
ENST00000399668.6:c.1611C>T	ENSP00000382576.2:p.Asn537=
ENST00000527044.5:c.1611C>T	ENSP00000432654.2:p.Asn537=
ENST00000533001.1:n.1756C>T
ENST00000534204.1:c.116-7449C>T	ENSP00000453857.1:n.116-7449C>T
ENST00000614337.4:n.1927C>T
NM_144508.4:c.1611C>T	NP_653091.3:p.Asn537=
NM_170589.4:c.1689C>T	NP_733468.3:p.Asn563=
XM_011521816.1:c.1287C>T	XP_011520118.1:p.Asn429=
XM_011521817.1:c.1611C>T	XP_011520119.1:p.Asn537=
XM_017022432.1:c.1287C>T	XP_016877921.1:p.Asn429=
NM_144508.5:c.1611C>T MANE Select	NP_653091.3:p.Asn537=
NM_170589.5:c.1689C>T	NP_733468.3:p.Asn563=