Canonical Allele Identifier: CA2678467019
Gene: CDKN1A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.36684524dup , CM000668.2:g.36684524dup GRCh38
NC_000006.11:g.36652301dup , CM000668.1:g.36652301dup GRCh37
NC_000006.10:g.36760279dup NCBI36
NG_009364.1:g.10843dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000244741.10:c.423dup MANE Select ENSP00000244741.6:p.Arg142ThrfsTer?
ENST00000244741.9:c.423dup ENSP00000244741.5:p.Arg142ThrfsTer?
ENST00000373711.3:c.423dup ENSP00000362815.1:p.Arg142ThrfsTer?
ENST00000405375.5:c.423dup ENSP00000384849.1:p.Arg142ThrfsTer?
ENST00000448526.6:c.423dup ENSP00000409259.3:p.Arg142ThrfsTer?
ENST00000615513.4:c.423dup ENSP00000482768.1:p.Arg142ThrfsTer?
NM_000389.4:c.423dup NP_000380.1:p.Arg142ThrfsTer?
NM_001220777.1:c.423dup NP_001207706.1:p.Arg142ThrfsTer?
NM_001220778.1:c.423dup NP_001207707.1:p.Arg142ThrfsTer?
NM_001291549.1:c.525dup NP_001278478.1:p.Arg176ThrfsTer?
NM_078467.2:c.423dup NP_510867.1:p.Arg142ThrfsTer?
NM_000389.5:c.423dup MANE Select NP_000380.1:p.Arg142ThrfsTer?
NM_001220777.2:c.423dup NP_001207706.1:p.Arg142ThrfsTer?
NM_001220778.2:c.423dup NP_001207707.1:p.Arg142ThrfsTer?
NM_001291549.3:c.525dup NP_001278478.1:p.Arg176ThrfsTer?
NM_001374509.1:c.525dup NP_001361438.1:p.Arg176ThrfsTer?
NM_001374510.1:c.462dup NP_001361439.1:p.Arg155ThrfsTer?
NM_001374511.1:c.423dup NP_001361440.1:p.Arg142ThrfsTer18
NM_001374512.1:c.423dup NP_001361441.1:p.Arg142ThrfsTer?
NM_001374513.1:c.423dup NP_001361442.1:p.Arg142ThrfsTer?
NM_078467.3:c.423dup NP_510867.1:p.Arg142ThrfsTer?