Canonical Allele Identifier: CA1969112174
Gene: CKAP5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.46827555T= , CM000673.2:g.46827555T= GRCh38
NC_000011.9:g.46849106T= , CM000673.1:g.46849106T= GRCh37
NC_000011.8:g.46805682T= NCBI36
NG_029924.1:g.23754A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000529230.6:c.-37-6287A= MANE Select ENSP00000432768.1:n.-37-6287A=
ENST00000312055.9:c.-37-6287A= ENSP00000310227.5:n.-37-6287A=
ENST00000525248.1:n.78-6307A=
ENST00000529230.5:c.-37-6287A= ENSP00000432768.1:n.-37-6287A=
NM_001008938.3:c.-37-6287A= NP_001008938.1:n.-37-6287A=
NM_014756.3:c.-37-6287A= NP_055571.2:n.-37-6287A=
NM_001008938.4:c.-37-6287A= MANE Select NP_001008938.1:n.-37-6287A=
NM_014756.4:c.-37-6287A= NP_055571.2:n.-37-6287A=