Canonical Allele Identifier: CA2171877462
Gene: KNL1 HGNC NCBI

Linked Data

dbSNP Id: rs1893561143

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.40651457G>A , CM000677.2:g.40651457G>A GRCh38
NC_000015.9:g.40943655G>A , CM000677.1:g.40943655G>A GRCh37
NC_000015.8:g.38730947G>A NCBI36
NG_033114.1:g.62209G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000399668.7:c.6213-14G>A MANE Select ENSP00000382576.3:n.6213-14G>A
ENST00000346991.9:c.6291-14G>A ENSP00000335463.6:n.6291-14G>A
ENST00000399668.6:c.6213-14G>A ENSP00000382576.2:n.6213-14G>A
ENST00000526913.5:c.3346-14G>A
ENST00000532347.1:n.293-14G>A
NM_144508.4:c.6213-14G>A NP_653091.3:n.6213-14G>A
NM_170589.4:c.6291-14G>A NP_733468.3:n.6291-14G>A
XM_011521816.1:c.5889-14G>A XP_011520118.1:n.5889-14G>A
XM_011521817.1:c.6213-14G>A XP_011520119.1:n.6213-14G>A
XM_017022432.1:c.5889-14G>A XP_016877921.1:n.5889-14G>A
NM_144508.5:c.6213-14G>A MANE Select NP_653091.3:n.6213-14G>A
NM_170589.5:c.6291-14G>A NP_733468.3:n.6291-14G>A