Canonical Allele Identifier: CA2578600461
Gene: CDKN1A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.36684584_36684587del , CM000668.2:g.36684584_36684587del GRCh38
NC_000006.11:g.36652361_36652364del , CM000668.1:g.36652361_36652364del GRCh37
NC_000006.10:g.36760339_36760342del NCBI36
NG_009364.1:g.10903_10906del

Transcript Alleles

HGVS Amino-acid Change
ENST00000244741.10:c.445+38_445+41del MANE Select ENSP00000244741.6:n.445+38_445+41del
ENST00000244741.9:c.445+38_445+41del ENSP00000244741.5:n.445+38_445+41del
ENST00000373711.3:c.445+38_445+41del ENSP00000362815.1:n.445+38_445+41del
ENST00000405375.5:c.445+38_445+41del ENSP00000384849.1:n.445+38_445+41del
ENST00000448526.6:c.445+38_445+41del ENSP00000409259.3:n.445+38_445+41del
ENST00000615513.4:c.445+38_445+41del ENSP00000482768.1:n.445+38_445+41del
NM_000389.4:c.445+38_445+41del NP_000380.1:n.445+38_445+41del
NM_001220777.1:c.445+38_445+41del NP_001207706.1:n.445+38_445+41del
NM_001220778.1:c.445+38_445+41del NP_001207707.1:n.445+38_445+41del
NM_001291549.1:c.547+38_547+41del NP_001278478.1:n.547+38_547+41del
NM_078467.2:c.445+38_445+41del NP_510867.1:n.445+38_445+41del
NM_000389.5:c.445+38_445+41del MANE Select NP_000380.1:n.445+38_445+41del
NM_001220777.2:c.445+38_445+41del NP_001207706.1:n.445+38_445+41del
NM_001220778.2:c.445+38_445+41del NP_001207707.1:n.445+38_445+41del
NM_001291549.3:c.547+38_547+41del NP_001278478.1:n.547+38_547+41del
NM_001374509.1:c.547+38_547+41del NP_001361438.1:n.547+38_547+41del
NM_001374510.1:c.484+38_484+41del NP_001361439.1:n.484+38_484+41del
NM_001374511.1:c.483_486del NP_001361440.1:p.Gly162SerfsTer9
NM_001374512.1:c.445+38_445+41del NP_001361441.1:n.445+38_445+41del
NM_001374513.1:c.445+38_445+41del NP_001361442.1:n.445+38_445+41del
NM_078467.3:c.445+38_445+41del NP_510867.1:n.445+38_445+41del