Canonical Allele Identifier: CA1969112214
Gene: CKAP5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.46827628_46827631delinsGAAA , CM000673.2:g.46827628_46827631delinsGAAA GRCh38
NC_000011.9:g.46849179_46849182delinsGAAA , CM000673.1:g.46849179_46849182delinsGAAA GRCh37
NC_000011.8:g.46805755_46805758delinsGAAA NCBI36
NG_029924.1:g.23678_23681delinsTTTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000529230.6:c.-37-6363_-37-6360delinsTTTC MANE Select ENSP00000432768.1:n.-37-6363_-37-6360delinsTTTC
ENST00000312055.9:c.-37-6363_-37-6360delinsTTTC ENSP00000310227.5:n.-37-6363_-37-6360delinsTTTC
ENST00000525248.1:n.78-6383_78-6380delinsTTTC
ENST00000529230.5:c.-37-6363_-37-6360delinsTTTC ENSP00000432768.1:n.-37-6363_-37-6360delinsTTTC
NM_001008938.3:c.-37-6363_-37-6360delinsTTTC NP_001008938.1:n.-37-6363_-37-6360delinsTTTC
NM_014756.3:c.-37-6363_-37-6360delinsTTTC NP_055571.2:n.-37-6363_-37-6360delinsTTTC
NM_001008938.4:c.-37-6363_-37-6360delinsTTTC MANE Select NP_001008938.1:n.-37-6363_-37-6360delinsTTTC
NM_014756.4:c.-37-6363_-37-6360delinsTTTC NP_055571.2:n.-37-6363_-37-6360delinsTTTC