Canonical Allele Identifier: CA1969112263
Gene: CKAP5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.46827776_46827777delinsAT , CM000673.2:g.46827776_46827777delinsAT GRCh38
NC_000011.9:g.46849327_46849328delinsAT , CM000673.1:g.46849327_46849328delinsAT GRCh37
NC_000011.8:g.46805903_46805904delinsAT NCBI36
NG_029924.1:g.23532_23533delinsAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000529230.6:c.-37-6509_-37-6508delinsAT MANE Select ENSP00000432768.1:n.-37-6509_-37-6508delinsAT
ENST00000312055.9:c.-37-6509_-37-6508delinsAT ENSP00000310227.5:n.-37-6509_-37-6508delinsAT
ENST00000525248.1:n.78-6529_78-6528delinsAT
ENST00000529230.5:c.-37-6509_-37-6508delinsAT ENSP00000432768.1:n.-37-6509_-37-6508delinsAT
NM_001008938.3:c.-37-6509_-37-6508delinsAT NP_001008938.1:n.-37-6509_-37-6508delinsAT
NM_014756.3:c.-37-6509_-37-6508delinsAT NP_055571.2:n.-37-6509_-37-6508delinsAT
NM_001008938.4:c.-37-6509_-37-6508delinsAT MANE Select NP_001008938.1:n.-37-6509_-37-6508delinsAT
NM_014756.4:c.-37-6509_-37-6508delinsAT NP_055571.2:n.-37-6509_-37-6508delinsAT