Canonical Allele Identifier: CA363834825
Gene: CDKN1A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.36685790G>T , CM000668.2:g.36685790G>T GRCh38
NC_000006.11:g.36653567G>T , CM000668.1:g.36653567G>T GRCh37
NC_000006.10:g.36761545G>T NCBI36
NG_009364.1:g.12109G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000244741.10:c.485G>T MANE Select ENSP00000244741.6:p.Arg162Met
ENST00000244741.9:c.485G>T ENSP00000244741.5:p.Arg162Met
ENST00000373711.3:c.485G>T ENSP00000362815.1:p.Arg162Met
ENST00000405375.5:c.485G>T ENSP00000384849.1:p.Arg162Met
ENST00000448526.6:c.485G>T ENSP00000409259.3:p.Arg162Met
ENST00000615513.4:c.485G>T ENSP00000482768.1:p.Arg162Met
NM_000389.4:c.485G>T NP_000380.1:p.Arg162Met
NM_001220777.1:c.485G>T NP_001207706.1:p.Arg162Met
NM_001220778.1:c.485G>T NP_001207707.1:p.Arg162Met
NM_001291549.1:c.587G>T NP_001278478.1:p.Arg196Met
NM_078467.2:c.485G>T NP_510867.1:p.Arg162Met
NM_000389.5:c.485G>T MANE Select NP_000380.1:p.Arg162Met
NM_001220777.2:c.485G>T NP_001207706.1:p.Arg162Met
NM_001220778.2:c.485G>T NP_001207707.1:p.Arg162Met
NM_001291549.3:c.587G>T NP_001278478.1:p.Arg196Met
NM_001374509.1:c.587G>T NP_001361438.1:p.Arg196Met
NM_001374510.1:c.524G>T NP_001361439.1:p.Arg175Met
NM_001374511.1:c.584G>T NP_001361440.1:p.Arg195Met
NM_001374512.1:c.*280G>T NP_001361441.1:n.*280G>T
NM_001374513.1:c.485G>T NP_001361442.1:p.Arg162Met
NM_078467.3:c.485G>T NP_510867.1:p.Arg162Met