Canonical Allele Identifier: CA2575680585
Gene: KNL1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.40651639G>T , CM000677.2:g.40651639G>T GRCh38
NC_000015.9:g.40943837G>T , CM000677.1:g.40943837G>T GRCh37
NC_000015.8:g.38731129G>T NCBI36
NG_033114.1:g.62391G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000399668.7:c.6314+67G>T MANE Select ENSP00000382576.3:n.6314+67G>T
ENST00000346991.9:c.6392+67G>T ENSP00000335463.6:n.6392+67G>T
ENST00000399668.6:c.6314+67G>T ENSP00000382576.2:n.6314+67G>T
ENST00000526913.5:c.3447+67G>T
ENST00000532347.1:n.394+67G>T
NM_144508.4:c.6314+67G>T NP_653091.3:n.6314+67G>T
NM_170589.4:c.6392+67G>T NP_733468.3:n.6392+67G>T
XM_011521816.1:c.5990+67G>T XP_011520118.1:n.5990+67G>T
XM_011521817.1:c.6314+67G>T XP_011520119.1:n.6314+67G>T
XM_017022432.1:c.5990+67G>T XP_016877921.1:n.5990+67G>T
NM_144508.5:c.6314+67G>T MANE Select NP_653091.3:n.6314+67G>T
NM_170589.5:c.6392+67G>T NP_733468.3:n.6392+67G>T