Canonical Allele Identifier: CA3780447
Gene: CDKN1A HGNC NCBI

Linked Data

dbSNP Id: rs1059234

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.36685820C>T , CM000668.2:g.36685820C>T GRCh38
NC_000006.11:g.36653597C>T , CM000668.1:g.36653597C>T GRCh37
NC_000006.10:g.36761575C>T NCBI36
NG_009364.1:g.12139C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000244741.10:c.*20C>T MANE Select ENSP00000244741.6:n.*20C>T
ENST00000244741.9:c.*20C>T ENSP00000244741.5:n.*20C>T
ENST00000373711.3:c.*20C>T ENSP00000362815.1:n.*20C>T
ENST00000405375.5:c.*20C>T ENSP00000384849.1:n.*20C>T
ENST00000448526.6:c.*20C>T ENSP00000409259.3:n.*20C>T
ENST00000615513.4:c.*20C>T ENSP00000482768.1:n.*20C>T
NM_000389.4:c.*20C>T NP_000380.1:n.*20C>T
NM_001220777.1:c.*20C>T NP_001207706.1:n.*20C>T
NM_001220778.1:c.*20C>T NP_001207707.1:n.*20C>T
NM_001291549.1:c.*20C>T NP_001278478.1:n.*20C>T
NM_078467.2:c.*20C>T NP_510867.1:n.*20C>T
NM_000389.5:c.*20C>T MANE Select NP_000380.1:n.*20C>T
NM_001220777.2:c.*20C>T NP_001207706.1:n.*20C>T
NM_001220778.2:c.*20C>T NP_001207707.1:n.*20C>T
NM_001291549.3:c.*20C>T NP_001278478.1:n.*20C>T
NM_001374509.1:c.*20C>T NP_001361438.1:n.*20C>T
NM_001374510.1:c.*20C>T NP_001361439.1:n.*20C>T
NM_001374511.1:c.*20C>T NP_001361440.1:n.*20C>T
NM_001374512.1:c.*310C>T NP_001361441.1:n.*310C>T
NM_001374513.1:c.*20C>T NP_001361442.1:n.*20C>T
NM_078467.3:c.*20C>T NP_510867.1:n.*20C>T