Canonical Allele Identifier: CA391731867
Gene: KNL1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.40621728G>C , CM000677.2:g.40621728G>C GRCh38
NC_000015.9:g.40913926G>C , CM000677.1:g.40913926G>C GRCh37
NC_000015.8:g.38701218G>C NCBI36
NG_033114.1:g.32480G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000399668.7:c.1464G>C MANE Select ENSP00000382576.3:p.Lys488Asn
ENST00000346991.9:c.1542G>C ENSP00000335463.6:p.Lys514Asn
ENST00000399668.6:c.1464G>C ENSP00000382576.2:p.Lys488Asn
ENST00000527044.5:c.1464G>C ENSP00000432654.2:p.Lys488Asn
ENST00000533001.1:n.1609G>C
ENST00000534204.1:c.116-7596G>C ENSP00000453857.1:n.116-7596G>C
ENST00000614337.4:n.1780G>C
NM_144508.4:c.1464G>C NP_653091.3:p.Lys488Asn
NM_170589.4:c.1542G>C NP_733468.3:p.Lys514Asn
XM_011521816.1:c.1140G>C XP_011520118.1:p.Lys380Asn
XM_011521817.1:c.1464G>C XP_011520119.1:p.Lys488Asn
XM_017022432.1:c.1140G>C XP_016877921.1:p.Lys380Asn
NM_144508.5:c.1464G>C MANE Select NP_653091.3:p.Lys488Asn
NM_170589.5:c.1542G>C NP_733468.3:p.Lys514Asn