Canonical Allele Identifier: CA348297719
Gene: CKAP2L HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.113514285T>G (hg19) chr2:g.112756708T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.112756708T>G , CM000664.2:g.112756708T>G GRCh38
NC_000002.11:g.113514285T>G , CM000664.1:g.113514285T>G GRCh37
NC_000002.10:g.113230756T>G NCBI36
NG_041820.1:g.12970A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000302450.11:c.663A>C MANE Select ENSP00000305204.6:p.Leu221Phe
ENST00000302450.10:c.663A>C ENSP00000305204.6:p.Leu221Phe
ENST00000435431.5:c.478+185A>C ENSP00000414834.1:n.478+185A>C
NM_001304361.1:c.168A>C NP_001291290.1:p.Leu56Phe
NM_152515.4:c.663A>C NP_689728.3:p.Leu221Phe
NR_130712.1:n.557+185A>C
XM_011510666.1:c.168A>C XP_011508968.1:p.Leu56Phe
XM_011510666.2:c.168A>C XP_011508968.1:p.Leu56Phe
NM_152515.5:c.663A>C MANE Select NP_689728.3:p.Leu221Phe
NM_001304361.2:c.168A>C NP_001291290.1:p.Leu56Phe
NR_130712.2:n.489+185A>C
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