Canonical Allele Identifier: CA566531958
Gene: CDKN1A HGNC NCBI

Linked Data

dbSNP Id: rs762424928
gnomAD v2: 6-36653513-G-C
gnomAD v4: 6-36685736-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.36685736G>C , CM000668.2:g.36685736G>C GRCh38
NC_000006.11:g.36653513G>C , CM000668.1:g.36653513G>C GRCh37
NC_000006.10:g.36761491G>C NCBI36
NG_009364.1:g.12055G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000244741.10:c.446-15G>C MANE Select ENSP00000244741.6:n.446-15G>C
ENST00000244741.9:c.446-15G>C ENSP00000244741.5:n.446-15G>C
ENST00000373711.3:c.446-15G>C ENSP00000362815.1:n.446-15G>C
ENST00000405375.5:c.446-15G>C ENSP00000384849.1:n.446-15G>C
ENST00000448526.6:c.446-15G>C ENSP00000409259.3:n.446-15G>C
ENST00000615513.4:c.446-15G>C ENSP00000482768.1:n.446-15G>C
NM_000389.4:c.446-15G>C NP_000380.1:n.446-15G>C
NM_001220777.1:c.446-15G>C NP_001207706.1:n.446-15G>C
NM_001220778.1:c.446-15G>C NP_001207707.1:n.446-15G>C
NM_001291549.1:c.548-15G>C NP_001278478.1:n.548-15G>C
NM_078467.2:c.446-15G>C NP_510867.1:n.446-15G>C
NM_000389.5:c.446-15G>C MANE Select NP_000380.1:n.446-15G>C
NM_001220777.2:c.446-15G>C NP_001207706.1:n.446-15G>C
NM_001220778.2:c.446-15G>C NP_001207707.1:n.446-15G>C
NM_001291549.3:c.548-15G>C NP_001278478.1:n.548-15G>C
NM_001374509.1:c.548-15G>C NP_001361438.1:n.548-15G>C
NM_001374510.1:c.485-15G>C NP_001361439.1:n.485-15G>C
NM_001374511.1:c.545-15G>C NP_001361440.1:n.545-15G>C
NM_001374512.1:c.*226G>C NP_001361441.1:n.*226G>C
NM_001374513.1:c.446-15G>C NP_001361442.1:n.446-15G>C
NM_078467.3:c.446-15G>C NP_510867.1:n.446-15G>C