Canonical Allele Identifier: CA268822952

Gene: KNL1

Linked Data

• dbSNP Id: rs997360736
• gnomAD v2: 15-40913718-A-C
• gnomAD v4: 15-40621520-A-C
• MyVariant Identifiers: chr15:g.40913718A>C (hg19) ; chr15:g.40621520A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40621520A>C , CM000677.2:g.40621520A>C	GRCh38
NC_000015.9:g.40913718A>C , CM000677.1:g.40913718A>C	GRCh37
NC_000015.8:g.38701010A>C	NCBI36
NG_033114.1:g.32272A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399668.7:c.1256A>C MANE Select	ENSP00000382576.3:p.Asn419Thr
ENST00000346991.9:c.1334A>C	ENSP00000335463.6:p.Asn445Thr
ENST00000399668.6:c.1256A>C	ENSP00000382576.2:p.Asn419Thr
ENST00000527044.5:c.1256A>C	ENSP00000432654.2:p.Asn419Thr
ENST00000533001.1:n.1401A>C
ENST00000534204.1:c.116-7804A>C	ENSP00000453857.1:n.116-7804A>C
ENST00000614337.4:n.1572A>C
NM_144508.4:c.1256A>C	NP_653091.3:p.Asn419Thr
NM_170589.4:c.1334A>C	NP_733468.3:p.Asn445Thr
XM_011521816.1:c.932A>C	XP_011520118.1:p.Asn311Thr
XM_011521817.1:c.1256A>C	XP_011520119.1:p.Asn419Thr
XM_017022432.1:c.932A>C	XP_016877921.1:p.Asn311Thr
NM_144508.5:c.1256A>C MANE Select	NP_653091.3:p.Asn419Thr
NM_170589.5:c.1334A>C	NP_733468.3:p.Asn445Thr