Canonical Allele Identifier: CA599043738
Gene: CKAP5 HGNC NCBI

Linked Data

dbSNP Id: rs1476254214
gnomAD v2: 11-46849434-TTTGTAG-T
MyVariant Identifiers: chr11:g.46849435_46849440del (hg19) chr11:g.46827884_46827889del (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.46827884_46827889del , CM000673.2:g.46827884_46827889del GRCh38
NC_000011.9:g.46849435_46849440del , CM000673.1:g.46849435_46849440del GRCh37
NC_000011.8:g.46806011_46806016del NCBI36
NG_029924.1:g.23420_23425del

Transcript Alleles

HGVS Amino-acid Change
ENST00000529230.6:c.-37-6621_-37-6616del MANE Select ENSP00000432768.1:n.-37-6621_-37-6616del
ENST00000312055.9:c.-37-6621_-37-6616del ENSP00000310227.5:n.-37-6621_-37-6616del
ENST00000525248.1:n.78-6641_78-6636del
ENST00000529230.5:c.-37-6621_-37-6616del ENSP00000432768.1:n.-37-6621_-37-6616del
NM_001008938.3:c.-37-6621_-37-6616del NP_001008938.1:n.-37-6621_-37-6616del
NM_014756.3:c.-37-6621_-37-6616del NP_055571.2:n.-37-6621_-37-6616del
NM_001008938.4:c.-37-6621_-37-6616del MANE Select NP_001008938.1:n.-37-6621_-37-6616del
NM_014756.4:c.-37-6621_-37-6616del NP_055571.2:n.-37-6621_-37-6616del
Search 100 bp 5'
Search 100 bp 3'