Canonical Allele Identifier: CA824303476
Gene: CDKN1A HGNC NCBI

Linked Data

dbSNP Id: rs1423988118
gnomAD v3: 6-36685847-G-A
gnomAD v4: 6-36685847-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.36685847G>A , CM000668.2:g.36685847G>A GRCh38
NC_000006.11:g.36653624G>A , CM000668.1:g.36653624G>A GRCh37
NC_000006.10:g.36761602G>A NCBI36
NG_009364.1:g.12166G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000244741.10:c.*47G>A MANE Select ENSP00000244741.6:n.*47G>A
ENST00000244741.9:c.*47G>A ENSP00000244741.5:n.*47G>A
ENST00000373711.3:c.*47G>A ENSP00000362815.1:n.*47G>A
ENST00000405375.5:c.*47G>A ENSP00000384849.1:n.*47G>A
ENST00000448526.6:c.*47G>A ENSP00000409259.3:n.*47G>A
ENST00000615513.4:c.*47G>A ENSP00000482768.1:n.*47G>A
NM_000389.4:c.*47G>A NP_000380.1:n.*47G>A
NM_001220777.1:c.*47G>A NP_001207706.1:n.*47G>A
NM_001220778.1:c.*47G>A NP_001207707.1:n.*47G>A
NM_001291549.1:c.*47G>A NP_001278478.1:n.*47G>A
NM_078467.2:c.*47G>A NP_510867.1:n.*47G>A
NM_000389.5:c.*47G>A MANE Select NP_000380.1:n.*47G>A
NM_001220777.2:c.*47G>A NP_001207706.1:n.*47G>A
NM_001220778.2:c.*47G>A NP_001207707.1:n.*47G>A
NM_001291549.3:c.*47G>A NP_001278478.1:n.*47G>A
NM_001374509.1:c.*47G>A NP_001361438.1:n.*47G>A
NM_001374510.1:c.*47G>A NP_001361439.1:n.*47G>A
NM_001374511.1:c.*47G>A NP_001361440.1:n.*47G>A
NM_001374512.1:c.*337G>A NP_001361441.1:n.*337G>A
NM_001374513.1:c.*47G>A NP_001361442.1:n.*47G>A
NM_078467.3:c.*47G>A NP_510867.1:n.*47G>A