Canonical Allele Identifier: CA1279906583
Gene: CKAP2L HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.112756865A= , CM000664.2:g.112756865A= GRCh38
NC_000002.11:g.113514442A= , CM000664.1:g.113514442A= GRCh37
NC_000002.10:g.113230913A= NCBI36
NG_041820.1:g.12813T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000302450.11:c.506T= MANE Select ENSP00000305204.6:p.Ile169=
ENST00000302450.10:c.506T= ENSP00000305204.6:p.Ile169=
ENST00000435431.5:c.478+28T= ENSP00000414834.1:n.478+28T=
ENST00000481732.5:n.467T=
NM_001304361.1:c.11T= NP_001291290.1:p.Ile4=
NM_152515.4:c.506T= NP_689728.3:p.Ile169=
NR_130712.1:n.557+28T=
XM_011510666.1:c.11T= XP_011508968.1:p.Ile4=
XM_011510666.2:c.11T= XP_011508968.1:p.Ile4=
NM_152515.5:c.506T= MANE Select NP_689728.3:p.Ile169=
NM_001304361.2:c.11T= NP_001291290.1:p.Ile4=
NR_130712.2:n.489+28T=