Canonical Allele Identifier: CA645558386
Gene: CDKN1A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.36684136_36684140del , CM000668.2:g.36684136_36684140del GRCh38
NC_000006.11:g.36651913_36651917del , CM000668.1:g.36651913_36651917del GRCh37
NC_000006.10:g.36759891_36759895del NCBI36
NG_009364.1:g.10455_10459del

Transcript Alleles

HGVS Amino-acid Change
ENST00000244741.10:c.35_39del MANE Select ENSP00000244741.6:p.Pro12ArgfsTer22
ENST00000244741.9:c.35_39del ENSP00000244741.5:p.Pro12ArgfsTer22
ENST00000373711.3:c.35_39del ENSP00000362815.1:p.Pro12ArgfsTer22
ENST00000405375.5:c.35_39del ENSP00000384849.1:p.Pro12ArgfsTer22
ENST00000448526.6:c.35_39del ENSP00000409259.3:p.Pro12ArgfsTer22
ENST00000459970.1:n.229_233del
ENST00000478800.1:n.254_258del
ENST00000615513.4:c.35_39del ENSP00000482768.1:p.Pro12ArgfsTer22
NM_000389.4:c.35_39del NP_000380.1:p.Pro12ArgfsTer22
NM_001220777.1:c.35_39del NP_001207706.1:p.Pro12ArgfsTer22
NM_001220778.1:c.35_39del NP_001207707.1:p.Pro12ArgfsTer22
NM_001291549.1:c.137_141del NP_001278478.1:p.Pro46ArgfsTer22
NM_078467.2:c.35_39del NP_510867.1:p.Pro12ArgfsTer22
NM_000389.5:c.35_39del MANE Select NP_000380.1:p.Pro12ArgfsTer22
NM_001220777.2:c.35_39del NP_001207706.1:p.Pro12ArgfsTer22
NM_001220778.2:c.35_39del NP_001207707.1:p.Pro12ArgfsTer22
NM_001291549.3:c.137_141del NP_001278478.1:p.Pro46ArgfsTer22
NM_001374509.1:c.137_141del NP_001361438.1:p.Pro46ArgfsTer22
NM_001374510.1:c.74_78del NP_001361439.1:p.Pro25ArgfsTer22
NM_001374511.1:c.35_39del NP_001361440.1:p.Pro12ArgfsTer22
NM_001374512.1:c.35_39del NP_001361441.1:p.Pro12ArgfsTer22
NM_001374513.1:c.35_39del NP_001361442.1:p.Pro12ArgfsTer22
NM_078467.3:c.35_39del NP_510867.1:p.Pro12ArgfsTer22