Canonical Allele Identifier: CA391731972
Gene: KNL1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.40621747G>T , CM000677.2:g.40621747G>T GRCh38
NC_000015.9:g.40913945G>T , CM000677.1:g.40913945G>T GRCh37
NC_000015.8:g.38701237G>T NCBI36
NG_033114.1:g.32499G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000399668.7:c.1483G>T MANE Select ENSP00000382576.3:p.Asp495Tyr
ENST00000346991.9:c.1561G>T ENSP00000335463.6:p.Asp521Tyr
ENST00000399668.6:c.1483G>T ENSP00000382576.2:p.Asp495Tyr
ENST00000527044.5:c.1483G>T ENSP00000432654.2:p.Asp495Tyr
ENST00000533001.1:n.1628G>T
ENST00000534204.1:c.116-7577G>T ENSP00000453857.1:n.116-7577G>T
ENST00000614337.4:n.1799G>T
NM_144508.4:c.1483G>T NP_653091.3:p.Asp495Tyr
NM_170589.4:c.1561G>T NP_733468.3:p.Asp521Tyr
XM_011521816.1:c.1159G>T XP_011520118.1:p.Asp387Tyr
XM_011521817.1:c.1483G>T XP_011520119.1:p.Asp495Tyr
XM_017022432.1:c.1159G>T XP_016877921.1:p.Asp387Tyr
NM_144508.5:c.1483G>T MANE Select NP_653091.3:p.Asp495Tyr
NM_170589.5:c.1561G>T NP_733468.3:p.Asp521Tyr