Canonical Allele Identifier: CA2171858592

Gene: KNL1

Linked Data

• dbSNP Id: rs913762622

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40611396C>G , CM000677.2:g.40611396C>G	GRCh38
NC_000015.9:g.40903594C>G , CM000677.1:g.40903594C>G	GRCh37
NC_000015.8:g.38690886C>G	NCBI36
NG_033114.1:g.22148C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000399668.7:c.251-82C>G MANE Select	ENSP00000382576.3:n.251-82C>G
ENST00000346991.9:c.329-82C>G	ENSP00000335463.6:n.329-82C>G
ENST00000399668.6:c.251-82C>G	ENSP00000382576.2:n.251-82C>G
ENST00000527044.5:c.251-82C>G	ENSP00000432654.2:n.251-82C>G
ENST00000533001.1:n.396-82C>G
ENST00000534204.1:c.115+4964C>G	ENSP00000453857.1:n.115+4964C>G
ENST00000614337.4:n.626-88C>G
NM_144508.4:c.251-82C>G	NP_653091.3:n.251-82C>G
NM_170589.4:c.329-82C>G	NP_733468.3:n.329-82C>G
XM_011521817.1:c.251-82C>G	XP_011520119.1:n.251-82C>G
XM_017022432.1:c.-41+1099C>G	XP_016877921.1:n.-41+1099C>G
NM_144508.5:c.251-82C>G MANE Select	NP_653091.3:n.251-82C>G
NM_170589.5:c.329-82C>G	NP_733468.3:n.329-82C>G