Canonical Allele Identifier: CA489773030
Gene: KNL1 HGNC NCBI

Linked Data

dbSNP Id: rs1893565330
MyVariant Identifiers: chr15:g.40943768G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.40651570G>A , CM000677.2:g.40651570G>A GRCh38
NC_000015.9:g.40943768G>A , CM000677.1:g.40943768G>A GRCh37
NC_000015.8:g.38731060G>A NCBI36
NG_033114.1:g.62322G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000399668.7:c.6312G>A MANE Select ENSP00000382576.3:p.Leu2104=
ENST00000346991.9:c.6390G>A ENSP00000335463.6:p.Leu2130=
ENST00000399668.6:c.6312G>A ENSP00000382576.2:p.Leu2104=
ENST00000526913.5:c.3445G>A
ENST00000532347.1:n.392G>A
NM_144508.4:c.6312G>A NP_653091.3:p.Leu2104=
NM_170589.4:c.6390G>A NP_733468.3:p.Leu2130=
XM_011521816.1:c.5988G>A XP_011520118.1:p.Leu1996=
XM_011521817.1:c.6312G>A XP_011520119.1:p.Leu2104=
XM_017022432.1:c.5988G>A XP_016877921.1:p.Leu1996=
NM_144508.5:c.6312G>A MANE Select NP_653091.3:p.Leu2104=
NM_170589.5:c.6390G>A NP_733468.3:p.Leu2130=