Canonical Allele Identifier: CA1969112222

Gene: CKAP5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46827636_46827637delinsGA , CM000673.2:g.46827636_46827637delinsGA	GRCh38
NC_000011.9:g.46849187_46849188delinsGA , CM000673.1:g.46849187_46849188delinsGA	GRCh37
NC_000011.8:g.46805763_46805764delinsGA	NCBI36
NG_029924.1:g.23672_23673delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529230.6:c.-37-6369_-37-6368delinsTC MANE Select	ENSP00000432768.1:n.-37-6369_-37-6368delinsTC
ENST00000312055.9:c.-37-6369_-37-6368delinsTC	ENSP00000310227.5:n.-37-6369_-37-6368delinsTC
ENST00000525248.1:n.78-6389_78-6388delinsTC
ENST00000529230.5:c.-37-6369_-37-6368delinsTC	ENSP00000432768.1:n.-37-6369_-37-6368delinsTC
NM_001008938.3:c.-37-6369_-37-6368delinsTC	NP_001008938.1:n.-37-6369_-37-6368delinsTC
NM_014756.3:c.-37-6369_-37-6368delinsTC	NP_055571.2:n.-37-6369_-37-6368delinsTC
NM_001008938.4:c.-37-6369_-37-6368delinsTC MANE Select	NP_001008938.1:n.-37-6369_-37-6368delinsTC
NM_014756.4:c.-37-6369_-37-6368delinsTC	NP_055571.2:n.-37-6369_-37-6368delinsTC