Canonical Allele Identifier: CA391773430
Gene: KNL1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.40651531A>C , CM000677.2:g.40651531A>C GRCh38
NC_000015.9:g.40943729A>C , CM000677.1:g.40943729A>C GRCh37
NC_000015.8:g.38731021A>C NCBI36
NG_033114.1:g.62283A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000399668.7:c.6273A>C MANE Select ENSP00000382576.3:p.Gln2091His
ENST00000346991.9:c.6351A>C ENSP00000335463.6:p.Gln2117His
ENST00000399668.6:c.6273A>C ENSP00000382576.2:p.Gln2091His
ENST00000526913.5:c.3406A>C
ENST00000532347.1:n.353A>C
NM_144508.4:c.6273A>C NP_653091.3:p.Gln2091His
NM_170589.4:c.6351A>C NP_733468.3:p.Gln2117His
XM_011521816.1:c.5949A>C XP_011520118.1:p.Gln1983His
XM_011521817.1:c.6273A>C XP_011520119.1:p.Gln2091His
XM_017022432.1:c.5949A>C XP_016877921.1:p.Gln1983His
NM_144508.5:c.6273A>C MANE Select NP_653091.3:p.Gln2091His
NM_170589.5:c.6351A>C NP_733468.3:p.Gln2117His