Canonical Allele Identifier: CA1969112226
Gene: CKAP5 HGNC NCBI

Linked Data

dbSNP Id: rs1939686559
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.46827648dup , CM000673.2:g.46827648dup GRCh38
NC_000011.9:g.46849199dup , CM000673.1:g.46849199dup GRCh37
NC_000011.8:g.46805775dup NCBI36
NG_029924.1:g.23662dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000529230.6:c.-37-6379dup MANE Select ENSP00000432768.1:n.-37-6379dup
ENST00000312055.9:c.-37-6379dup ENSP00000310227.5:n.-37-6379dup
ENST00000525248.1:n.78-6399dup
ENST00000529230.5:c.-37-6379dup ENSP00000432768.1:n.-37-6379dup
NM_001008938.3:c.-37-6379dup NP_001008938.1:n.-37-6379dup
NM_014756.3:c.-37-6379dup NP_055571.2:n.-37-6379dup
NM_001008938.4:c.-37-6379dup MANE Select NP_001008938.1:n.-37-6379dup
NM_014756.4:c.-37-6379dup NP_055571.2:n.-37-6379dup
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