Canonical Allele Identifier: CA712763553

Gene: KNL1

Linked Data

• dbSNP Id: rs1276485346
• gnomAD v4: 15-40651677-C-A
• MyVariant Identifiers: chr15:g.40943875C>A (hg19) ; chr15:g.40651677C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40651677C>A , CM000677.2:g.40651677C>A	GRCh38
NC_000015.9:g.40943875C>A , CM000677.1:g.40943875C>A	GRCh37
NC_000015.8:g.38731167C>A	NCBI36
NG_033114.1:g.62429C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399668.7:c.6314+105C>A MANE Select	ENSP00000382576.3:n.6314+105C>A
ENST00000346991.9:c.6392+105C>A	ENSP00000335463.6:n.6392+105C>A
ENST00000399668.6:c.6314+105C>A	ENSP00000382576.2:n.6314+105C>A
ENST00000526913.5:c.3447+105C>A
ENST00000532347.1:n.394+105C>A
NM_144508.4:c.6314+105C>A	NP_653091.3:n.6314+105C>A
NM_170589.4:c.6392+105C>A	NP_733468.3:n.6392+105C>A
XM_011521816.1:c.5990+105C>A	XP_011520118.1:n.5990+105C>A
XM_011521817.1:c.6314+105C>A	XP_011520119.1:n.6314+105C>A
XM_017022432.1:c.5990+105C>A	XP_016877921.1:n.5990+105C>A
NM_144508.5:c.6314+105C>A MANE Select	NP_653091.3:n.6314+105C>A
NM_170589.5:c.6392+105C>A	NP_733468.3:n.6392+105C>A