Canonical Allele Identifier: CA1969112114
Gene: CKAP5 HGNC NCBI

Linked Data

dbSNP Id: rs1939681132
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.46827414A>G , CM000673.2:g.46827414A>G GRCh38
NC_000011.9:g.46848965A>G , CM000673.1:g.46848965A>G GRCh37
NC_000011.8:g.46805541A>G NCBI36
NG_029924.1:g.23895T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000529230.6:c.-37-6146T>C MANE Select ENSP00000432768.1:n.-37-6146T>C
ENST00000312055.9:c.-37-6146T>C ENSP00000310227.5:n.-37-6146T>C
ENST00000525248.1:n.78-6166T>C
ENST00000529230.5:c.-37-6146T>C ENSP00000432768.1:n.-37-6146T>C
NM_001008938.3:c.-37-6146T>C NP_001008938.1:n.-37-6146T>C
NM_014756.3:c.-37-6146T>C NP_055571.2:n.-37-6146T>C
NM_001008938.4:c.-37-6146T>C MANE Select NP_001008938.1:n.-37-6146T>C
NM_014756.4:c.-37-6146T>C NP_055571.2:n.-37-6146T>C
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