Canonical Allele Identifier: CA348298121
Gene: CKAP2L HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.112756882T>C , CM000664.2:g.112756882T>C GRCh38
NC_000002.11:g.113514459T>C , CM000664.1:g.113514459T>C GRCh37
NC_000002.10:g.113230930T>C NCBI36
NG_041820.1:g.12796A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000302450.11:c.489A>G MANE Select ENSP00000305204.6:p.Ile163Met
ENST00000302450.10:c.489A>G ENSP00000305204.6:p.Ile163Met
ENST00000435431.5:c.478+11A>G ENSP00000414834.1:n.478+11A>G
ENST00000481732.5:n.450A>G
NM_001304361.1:c.-7A>G NP_001291290.1:n.-7A>G
NM_152515.4:c.489A>G NP_689728.3:p.Ile163Met
NR_130712.1:n.557+11A>G
XM_011510666.1:c.-7A>G XP_011508968.1:n.-7A>G
XM_011510666.2:c.-7A>G XP_011508968.1:n.-7A>G
NM_152515.5:c.489A>G MANE Select NP_689728.3:p.Ile163Met
NM_001304361.2:c.-7A>G NP_001291290.1:n.-7A>G
NR_130712.2:n.489+11A>G