Canonical Allele Identifier: CA391732209
Gene: KNL1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.40621778A>G , CM000677.2:g.40621778A>G GRCh38
NC_000015.9:g.40913976A>G , CM000677.1:g.40913976A>G GRCh37
NC_000015.8:g.38701268A>G NCBI36
NG_033114.1:g.32530A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000399668.7:c.1514A>G MANE Select ENSP00000382576.3:p.Asn505Ser
ENST00000346991.9:c.1592A>G ENSP00000335463.6:p.Asn531Ser
ENST00000399668.6:c.1514A>G ENSP00000382576.2:p.Asn505Ser
ENST00000527044.5:c.1514A>G ENSP00000432654.2:p.Asn505Ser
ENST00000533001.1:n.1659A>G
ENST00000534204.1:c.116-7546A>G ENSP00000453857.1:n.116-7546A>G
ENST00000614337.4:n.1830A>G
NM_144508.4:c.1514A>G NP_653091.3:p.Asn505Ser
NM_170589.4:c.1592A>G NP_733468.3:p.Asn531Ser
XM_011521816.1:c.1190A>G XP_011520118.1:p.Asn397Ser
XM_011521817.1:c.1514A>G XP_011520119.1:p.Asn505Ser
XM_017022432.1:c.1190A>G XP_016877921.1:p.Asn397Ser
NM_144508.5:c.1514A>G MANE Select NP_653091.3:p.Asn505Ser
NM_170589.5:c.1592A>G NP_733468.3:p.Asn531Ser