Canonical Allele Identifier: CA676946877
Gene: CKAP5 HGNC NCBI

Linked Data

dbSNP Id: rs1414443180
MyVariant Identifiers: chr11:g.46849274_46849277del (hg19) chr11:g.46827723_46827726del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.46827727_46827730del , CM000673.2:g.46827727_46827730del GRCh38
NC_000011.9:g.46849278_46849281del , CM000673.1:g.46849278_46849281del GRCh37
NC_000011.8:g.46805854_46805857del NCBI36
NG_029924.1:g.23583_23586del

Transcript Alleles

HGVS Amino-acid Change
ENST00000529230.6:c.-37-6458_-37-6455del MANE Select ENSP00000432768.1:n.-37-6458_-37-6455del
ENST00000312055.9:c.-37-6458_-37-6455del ENSP00000310227.5:n.-37-6458_-37-6455del
ENST00000525248.1:n.78-6478_78-6475del
ENST00000529230.5:c.-37-6458_-37-6455del ENSP00000432768.1:n.-37-6458_-37-6455del
NM_001008938.3:c.-37-6458_-37-6455del NP_001008938.1:n.-37-6458_-37-6455del
NM_014756.3:c.-37-6458_-37-6455del NP_055571.2:n.-37-6458_-37-6455del
NM_001008938.4:c.-37-6458_-37-6455del MANE Select NP_001008938.1:n.-37-6458_-37-6455del
NM_014756.4:c.-37-6458_-37-6455del NP_055571.2:n.-37-6458_-37-6455del
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