Canonical Allele Identifier: CA712763533

Gene: KNL1

Linked Data

• dbSNP Id: rs1281085068
• MyVariant Identifiers: chr15:g.40943818_40943819insG (hg19) ; chr15:g.40651620_40651621insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40651622dup , CM000677.2:g.40651622dup	GRCh38
NC_000015.9:g.40943820dup , CM000677.1:g.40943820dup	GRCh37
NC_000015.8:g.38731112dup	NCBI36
NG_033114.1:g.62374dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399668.7:c.6314+50dup MANE Select	ENSP00000382576.3:n.6314+50dup
ENST00000346991.9:c.6392+50dup	ENSP00000335463.6:n.6392+50dup
ENST00000399668.6:c.6314+50dup	ENSP00000382576.2:n.6314+50dup
ENST00000526913.5:c.3447+50dup
ENST00000532347.1:n.394+50dup
NM_144508.4:c.6314+50dup	NP_653091.3:n.6314+50dup
NM_170589.4:c.6392+50dup	NP_733468.3:n.6392+50dup
XM_011521816.1:c.5990+50dup	XP_011520118.1:n.5990+50dup
XM_011521817.1:c.6314+50dup	XP_011520119.1:n.6314+50dup
XM_017022432.1:c.5990+50dup	XP_016877921.1:n.5990+50dup
NM_144508.5:c.6314+50dup MANE Select	NP_653091.3:n.6314+50dup
NM_170589.5:c.6392+50dup	NP_733468.3:n.6392+50dup