Canonical Allele Identifier: CA1969112217
Gene: CKAP5 HGNC NCBI

Linked Data

dbSNP Id: rs988154621
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.46827635dup , CM000673.2:g.46827635dup GRCh38
NC_000011.9:g.46849186dup , CM000673.1:g.46849186dup GRCh37
NC_000011.8:g.46805762dup NCBI36
NG_029924.1:g.23680dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000529230.6:c.-37-6361dup MANE Select ENSP00000432768.1:n.-37-6361dup
ENST00000312055.9:c.-37-6361dup ENSP00000310227.5:n.-37-6361dup
ENST00000525248.1:n.78-6381dup
ENST00000529230.5:c.-37-6361dup ENSP00000432768.1:n.-37-6361dup
NM_001008938.3:c.-37-6361dup NP_001008938.1:n.-37-6361dup
NM_014756.3:c.-37-6361dup NP_055571.2:n.-37-6361dup
NM_001008938.4:c.-37-6361dup MANE Select NP_001008938.1:n.-37-6361dup
NM_014756.4:c.-37-6361dup NP_055571.2:n.-37-6361dup
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