Canonical Allele Identifier: CA16619923
Gene: KNL1 HGNC NCBI

Linked Data

dbSNP Id: rs1064795910
MyVariant Identifiers: chr15:g.40920835_40920836del (hg19) chr15:g.40628637_40628638del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.40628637_40628638del , CM000677.2:g.40628637_40628638del GRCh38
NC_000015.9:g.40920835_40920836del , CM000677.1:g.40920835_40920836del GRCh37
NC_000015.8:g.38708127_38708128del NCBI36
NG_033114.1:g.39389_39390del

Transcript Alleles

HGVS Amino-acid change
ENST00000399668.7:c.5542_5543del MANE Select ENSP00000382576.3:p.Gln1848ValfsTer8
ENST00000346991.9:c.5620_5621del ENSP00000335463.6:p.Gln1874ValfsTer8
ENST00000399668.6:c.5542_5543del ENSP00000382576.2:p.Gln1848ValfsTer8
ENST00000526913.5:c.2675_2676del
ENST00000532406.1:c.162_163del
ENST00000534204.1:c.116-687_116-686del ENSP00000453857.1:n.116-687_116-686del
NM_144508.4:c.5542_5543del NP_653091.3:p.Gln1848ValfsTer8
NM_170589.4:c.5620_5621del NP_733468.3:p.Gln1874ValfsTer8
XM_011521816.1:c.5218_5219del XP_011520118.1:p.Gln1740ValfsTer8
XM_011521817.1:c.5542_5543del XP_011520119.1:p.Gln1848ValfsTer8
XM_017022432.1:c.5218_5219del XP_016877921.1:p.Gln1740ValfsTer8
NM_144508.5:c.5542_5543del MANE Select NP_653091.3:p.Gln1848ValfsTer8
NM_170589.5:c.5620_5621del NP_733468.3:p.Gln1874ValfsTer8
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