Canonical Allele Identifier: CA1279906585
Gene: CKAP2L HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.112756873C= , CM000664.2:g.112756873C= GRCh38
NC_000002.11:g.113514450C= , CM000664.1:g.113514450C= GRCh37
NC_000002.10:g.113230921C= NCBI36
NG_041820.1:g.12805G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000302450.11:c.498G= MANE Select ENSP00000305204.6:p.Met166=
ENST00000302450.10:c.498G= ENSP00000305204.6:p.Met166=
ENST00000435431.5:c.478+20G= ENSP00000414834.1:n.478+20G=
ENST00000481732.5:n.459G=
NM_001304361.1:c.3G= NP_001291290.1:p.Met1=
NM_152515.4:c.498G= NP_689728.3:p.Met166=
NR_130712.1:n.557+20G=
XM_011510666.1:c.3G= XP_011508968.1:p.Met1=
XM_011510666.2:c.3G= XP_011508968.1:p.Met1=
NM_152515.5:c.498G= MANE Select NP_689728.3:p.Met166=
NM_001304361.2:c.3G= NP_001291290.1:p.Met1=
NR_130712.2:n.489+20G=