Canonical Allele Identifier: CA2171877469
Gene: KNL1 HGNC NCBI

Linked Data

dbSNP Id: rs1893561550

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.40651466T>G , CM000677.2:g.40651466T>G GRCh38
NC_000015.9:g.40943664T>G , CM000677.1:g.40943664T>G GRCh37
NC_000015.8:g.38730956T>G NCBI36
NG_033114.1:g.62218T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000399668.7:c.6213-5T>G MANE Select ENSP00000382576.3:n.6213-5T>G
ENST00000346991.9:c.6291-5T>G ENSP00000335463.6:n.6291-5T>G
ENST00000399668.6:c.6213-5T>G ENSP00000382576.2:n.6213-5T>G
ENST00000526913.5:c.3346-5T>G
ENST00000532347.1:n.293-5T>G
NM_144508.4:c.6213-5T>G NP_653091.3:n.6213-5T>G
NM_170589.4:c.6291-5T>G NP_733468.3:n.6291-5T>G
XM_011521816.1:c.5889-5T>G XP_011520118.1:n.5889-5T>G
XM_011521817.1:c.6213-5T>G XP_011520119.1:n.6213-5T>G
XM_017022432.1:c.5889-5T>G XP_016877921.1:n.5889-5T>G
NM_144508.5:c.6213-5T>G MANE Select NP_653091.3:n.6213-5T>G
NM_170589.5:c.6291-5T>G NP_733468.3:n.6291-5T>G