Canonical Allele Identifier: CA712757196

Gene: KNL1

Linked Data

• dbSNP Id: rs1303218548
• gnomAD v3: 15-40611399-G-A
• gnomAD v4: 15-40611399-G-A
• MyVariant Identifiers: chr15:g.40903597G>A (hg19) ; chr15:g.40611399G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40611399G>A , CM000677.2:g.40611399G>A	GRCh38
NC_000015.9:g.40903597G>A , CM000677.1:g.40903597G>A	GRCh37
NC_000015.8:g.38690889G>A	NCBI36
NG_033114.1:g.22151G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399668.7:c.251-79G>A MANE Select	ENSP00000382576.3:n.251-79G>A
ENST00000346991.9:c.329-79G>A	ENSP00000335463.6:n.329-79G>A
ENST00000399668.6:c.251-79G>A	ENSP00000382576.2:n.251-79G>A
ENST00000527044.5:c.251-79G>A	ENSP00000432654.2:n.251-79G>A
ENST00000533001.1:n.396-79G>A
ENST00000534204.1:c.115+4967G>A	ENSP00000453857.1:n.115+4967G>A
ENST00000614337.4:n.626-85G>A
NM_144508.4:c.251-79G>A	NP_653091.3:n.251-79G>A
NM_170589.4:c.329-79G>A	NP_733468.3:n.329-79G>A
XM_011521817.1:c.251-79G>A	XP_011520119.1:n.251-79G>A
XM_017022432.1:c.-41+1102G>A	XP_016877921.1:n.-41+1102G>A
NM_144508.5:c.251-79G>A MANE Select	NP_653091.3:n.251-79G>A
NM_170589.5:c.329-79G>A	NP_733468.3:n.329-79G>A