Canonical Allele Identifier: CA391773616
Gene: KNL1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.40651572G>C , CM000677.2:g.40651572G>C GRCh38
NC_000015.9:g.40943770G>C , CM000677.1:g.40943770G>C GRCh37
NC_000015.8:g.38731062G>C NCBI36
NG_033114.1:g.62324G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000399668.7:c.6314G>C MANE Select ENSP00000382576.3:p.Ser2105Thr
ENST00000346991.9:c.6392G>C ENSP00000335463.6:p.Ser2131Thr
ENST00000399668.6:c.6314G>C ENSP00000382576.2:p.Ser2105Thr
ENST00000526913.5:c.3447G>C
ENST00000532347.1:n.394G>C
NM_144508.4:c.6314G>C NP_653091.3:p.Ser2105Thr
NM_170589.4:c.6392G>C NP_733468.3:p.Ser2131Thr
XM_011521816.1:c.5990G>C XP_011520118.1:p.Ser1997Thr
XM_011521817.1:c.6314G>C XP_011520119.1:p.Ser2105Thr
XM_017022432.1:c.5990G>C XP_016877921.1:p.Ser1997Thr
NM_144508.5:c.6314G>C MANE Select NP_653091.3:p.Ser2105Thr
NM_170589.5:c.6392G>C NP_733468.3:p.Ser2131Thr