Canonical Allele Identifier: CA566531968
Gene: CDKN1A HGNC NCBI

Linked Data

dbSNP Id: rs1376040331

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.36685815dup , CM000668.2:g.36685815dup GRCh38
NC_000006.11:g.36653592dup , CM000668.1:g.36653592dup GRCh37
NC_000006.10:g.36761570dup NCBI36
NG_009364.1:g.12134dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000244741.10:c.*15dup MANE Select ENSP00000244741.6:n.*15dup
ENST00000244741.9:c.*15dup ENSP00000244741.5:n.*15dup
ENST00000373711.3:c.*15dup ENSP00000362815.1:n.*15dup
ENST00000405375.5:c.*15dup ENSP00000384849.1:n.*15dup
ENST00000448526.6:c.*15dup ENSP00000409259.3:n.*15dup
ENST00000615513.4:c.*15dup ENSP00000482768.1:n.*15dup
NM_000389.4:c.*15dup NP_000380.1:n.*15dup
NM_001220777.1:c.*15dup NP_001207706.1:n.*15dup
NM_001220778.1:c.*15dup NP_001207707.1:n.*15dup
NM_001291549.1:c.*15dup NP_001278478.1:n.*15dup
NM_078467.2:c.*15dup NP_510867.1:n.*15dup
NM_000389.5:c.*15dup MANE Select NP_000380.1:n.*15dup
NM_001220777.2:c.*15dup NP_001207706.1:n.*15dup
NM_001220778.2:c.*15dup NP_001207707.1:n.*15dup
NM_001291549.3:c.*15dup NP_001278478.1:n.*15dup
NM_001374509.1:c.*15dup NP_001361438.1:n.*15dup
NM_001374510.1:c.*15dup NP_001361439.1:n.*15dup
NM_001374511.1:c.*15dup NP_001361440.1:n.*15dup
NM_001374512.1:c.*305dup NP_001361441.1:n.*305dup
NM_001374513.1:c.*15dup NP_001361442.1:n.*15dup
NM_078467.3:c.*15dup NP_510867.1:n.*15dup