Canonical Allele Identifier: CA2582341694
Gene: CDKN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2582279
ClinVar RCV Id: RCV003332980

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.36684296_36684297delinsAA , CM000668.2:g.36684296_36684297delinsAA GRCh38
NC_000006.11:g.36652073_36652074delinsAA , CM000668.1:g.36652073_36652074delinsAA GRCh37
NC_000006.10:g.36760051_36760052delinsAA NCBI36
NG_009364.1:g.10615_10616delinsAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000244741.10:c.195_196delinsAA MANE Select ENSP00000244741.6:p.Trp65Ter
ENST00000244741.9:c.195_196delinsAA ENSP00000244741.5:p.Trp65Ter
ENST00000373711.3:c.195_196delinsAA ENSP00000362815.1:p.Trp65Ter
ENST00000405375.5:c.195_196delinsAA ENSP00000384849.1:p.Trp65Ter
ENST00000448526.6:c.195_196delinsAA ENSP00000409259.3:p.Trp65Ter
ENST00000459970.1:n.389_390delinsAA
ENST00000478800.1:n.414_415delinsAA
ENST00000615513.4:c.195_196delinsAA ENSP00000482768.1:p.Trp65Ter
NM_000389.4:c.195_196delinsAA NP_000380.1:p.Trp65Ter
NM_001220777.1:c.195_196delinsAA NP_001207706.1:p.Trp65Ter
NM_001220778.1:c.195_196delinsAA NP_001207707.1:p.Trp65Ter
NM_001291549.1:c.297_298delinsAA NP_001278478.1:p.Trp99Ter
NM_078467.2:c.195_196delinsAA NP_510867.1:p.Trp65Ter
NM_000389.5:c.195_196delinsAA MANE Select NP_000380.1:p.Trp65Ter
NM_001220777.2:c.195_196delinsAA NP_001207706.1:p.Trp65Ter
NM_001220778.2:c.195_196delinsAA NP_001207707.1:p.Trp65Ter
NM_001291549.3:c.297_298delinsAA NP_001278478.1:p.Trp99Ter
NM_001374509.1:c.297_298delinsAA NP_001361438.1:p.Trp99Ter
NM_001374510.1:c.234_235delinsAA NP_001361439.1:p.Trp78Ter
NM_001374511.1:c.195_196delinsAA NP_001361440.1:p.Trp65Ter
NM_001374512.1:c.195_196delinsAA NP_001361441.1:p.Trp65Ter
NM_001374513.1:c.195_196delinsAA NP_001361442.1:p.Trp65Ter
NM_078467.3:c.195_196delinsAA NP_510867.1:p.Trp65Ter