Canonical Allele Identifier: CA1969112229

Gene: CKAP5

Linked Data

• dbSNP Id: rs1939686721

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46827660_46827663del , CM000673.2:g.46827660_46827663del	GRCh38
NC_000011.9:g.46849211_46849214del , CM000673.1:g.46849211_46849214del	GRCh37
NC_000011.8:g.46805787_46805790del	NCBI36
NG_029924.1:g.23649_23652del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529230.6:c.-37-6392_-37-6389del MANE Select	ENSP00000432768.1:n.-37-6392_-37-6389del
ENST00000312055.9:c.-37-6392_-37-6389del	ENSP00000310227.5:n.-37-6392_-37-6389del
ENST00000525248.1:n.78-6412_78-6409del
ENST00000529230.5:c.-37-6392_-37-6389del	ENSP00000432768.1:n.-37-6392_-37-6389del
NM_001008938.3:c.-37-6392_-37-6389del	NP_001008938.1:n.-37-6392_-37-6389del
NM_014756.3:c.-37-6392_-37-6389del	NP_055571.2:n.-37-6392_-37-6389del
NM_001008938.4:c.-37-6392_-37-6389del MANE Select	NP_001008938.1:n.-37-6392_-37-6389del
NM_014756.4:c.-37-6392_-37-6389del	NP_055571.2:n.-37-6392_-37-6389del