Canonical Allele Identifier: CA645515831

Gene: CKAP2L

Linked Data

• COSMIC: COSM327351

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.112756877_112756878del , CM000664.2:g.112756877_112756878del	GRCh38
NC_000002.11:g.113514454_113514455del , CM000664.1:g.113514454_113514455del	GRCh37
NC_000002.10:g.113230925_113230926del	NCBI36
NG_041820.1:g.12801_12802del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302450.11:c.494_495del MANE Select	ENSP00000305204.6:p.Phe165TyrfsTer3
ENST00000302450.10:c.494_495del	ENSP00000305204.6:p.Phe165TyrfsTer3
ENST00000435431.5:c.478+16_478+17del	ENSP00000414834.1:n.478+16_478+17del
ENST00000481732.5:n.455_456del
NM_001304361.1:c.-2_-1del	NP_001291290.1:n.-2_-1del
NM_152515.4:c.494_495del	NP_689728.3:p.Phe165TyrfsTer3
NR_130712.1:n.557+16_557+17del
XM_011510666.1:c.-2_-1del	XP_011508968.1:n.-2_-1del
XM_011510666.2:c.-2_-1del	XP_011508968.1:n.-2_-1del
NM_152515.5:c.494_495del MANE Select	NP_689728.3:p.Phe165TyrfsTer3
NM_001304361.2:c.-2_-1del	NP_001291290.1:n.-2_-1del
NR_130712.2:n.489+16_489+17del