Canonical Allele Identifier: CA2838613789
Gene: CDKN1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.36685812dup , CM000668.2:g.36685812dup GRCh38
NC_000006.11:g.36653589dup , CM000668.1:g.36653589dup GRCh37
NC_000006.10:g.36761567dup NCBI36
NG_009364.1:g.12131dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000244741.10:c.*12dup MANE Select ENSP00000244741.6:n.*12dup
ENST00000244741.9:c.*12dup ENSP00000244741.5:n.*12dup
ENST00000373711.3:c.*12dup ENSP00000362815.1:n.*12dup
ENST00000405375.5:c.*12dup ENSP00000384849.1:n.*12dup
ENST00000448526.6:c.*12dup ENSP00000409259.3:n.*12dup
ENST00000615513.4:c.*12dup ENSP00000482768.1:n.*12dup
NM_000389.4:c.*12dup NP_000380.1:n.*12dup
NM_001220777.1:c.*12dup NP_001207706.1:n.*12dup
NM_001220778.1:c.*12dup NP_001207707.1:n.*12dup
NM_001291549.1:c.*12dup NP_001278478.1:n.*12dup
NM_078467.2:c.*12dup NP_510867.1:n.*12dup
NM_000389.5:c.*12dup MANE Select NP_000380.1:n.*12dup
NM_001220777.2:c.*12dup NP_001207706.1:n.*12dup
NM_001220778.2:c.*12dup NP_001207707.1:n.*12dup
NM_001291549.3:c.*12dup NP_001278478.1:n.*12dup
NM_001374509.1:c.*12dup NP_001361438.1:n.*12dup
NM_001374510.1:c.*12dup NP_001361439.1:n.*12dup
NM_001374511.1:c.*12dup NP_001361440.1:n.*12dup
NM_001374512.1:c.*302dup NP_001361441.1:n.*302dup
NM_001374513.1:c.*12dup NP_001361442.1:n.*12dup
NM_078467.3:c.*12dup NP_510867.1:n.*12dup