Canonical Allele Identifier: CA712763560

Gene: KNL1

Linked Data

• dbSNP Id: rs1239637293
• MyVariant Identifiers: chr15:g.40943897_40943898del (hg19) ; chr15:g.40651699_40651700del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40651701_40651702del , CM000677.2:g.40651701_40651702del	GRCh38
NC_000015.9:g.40943899_40943900del , CM000677.1:g.40943899_40943900del	GRCh37
NC_000015.8:g.38731191_38731192del	NCBI36
NG_033114.1:g.62453_62454del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399668.7:c.6314+129_6314+130del MANE Select	ENSP00000382576.3:n.6314+129_6314+130del
ENST00000346991.9:c.6392+129_6392+130del	ENSP00000335463.6:n.6392+129_6392+130del
ENST00000399668.6:c.6314+129_6314+130del	ENSP00000382576.2:n.6314+129_6314+130del
ENST00000526913.5:c.3447+129_3447+130del
ENST00000532347.1:n.394+129_394+130del
NM_144508.4:c.6314+129_6314+130del	NP_653091.3:n.6314+129_6314+130del
NM_170589.4:c.6392+129_6392+130del	NP_733468.3:n.6392+129_6392+130del
XM_011521816.1:c.5990+129_5990+130del	XP_011520118.1:n.5990+129_5990+130del
XM_011521817.1:c.6314+129_6314+130del	XP_011520119.1:n.6314+129_6314+130del
XM_017022432.1:c.5990+129_5990+130del	XP_016877921.1:n.5990+129_5990+130del
NM_144508.5:c.6314+129_6314+130del MANE Select	NP_653091.3:n.6314+129_6314+130del
NM_170589.5:c.6392+129_6392+130del	NP_733468.3:n.6392+129_6392+130del