Canonical Allele Identifier: CA2791317302
Gene: CKAP5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.46827505T>A , CM000673.2:g.46827505T>A GRCh38
NC_000011.9:g.46849056T>A , CM000673.1:g.46849056T>A GRCh37
NC_000011.8:g.46805632T>A NCBI36
NG_029924.1:g.23804A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000529230.6:c.-37-6237A>T MANE Select ENSP00000432768.1:n.-37-6237A>T
ENST00000312055.9:c.-37-6237A>T ENSP00000310227.5:n.-37-6237A>T
ENST00000525248.1:n.78-6257A>T
ENST00000529230.5:c.-37-6237A>T ENSP00000432768.1:n.-37-6237A>T
NM_001008938.3:c.-37-6237A>T NP_001008938.1:n.-37-6237A>T
NM_014756.3:c.-37-6237A>T NP_055571.2:n.-37-6237A>T
NM_001008938.4:c.-37-6237A>T MANE Select NP_001008938.1:n.-37-6237A>T
NM_014756.4:c.-37-6237A>T NP_055571.2:n.-37-6237A>T