Canonical Allele Identifier: CA2678467205
Gene: CDKN1A HGNC NCBI

Linked Data

gnomAD v4: 6-36685678-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.36685678G>T , CM000668.2:g.36685678G>T GRCh38
NC_000006.11:g.36653455G>T , CM000668.1:g.36653455G>T GRCh37
NC_000006.10:g.36761433G>T NCBI36
NG_009364.1:g.11997G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000244741.10:c.446-73G>T MANE Select ENSP00000244741.6:n.446-73G>T
ENST00000244741.9:c.446-73G>T ENSP00000244741.5:n.446-73G>T
ENST00000373711.3:c.446-73G>T ENSP00000362815.1:n.446-73G>T
ENST00000405375.5:c.446-73G>T ENSP00000384849.1:n.446-73G>T
ENST00000448526.6:c.446-73G>T ENSP00000409259.3:n.446-73G>T
ENST00000615513.4:c.446-73G>T ENSP00000482768.1:n.446-73G>T
NM_000389.4:c.446-73G>T NP_000380.1:n.446-73G>T
NM_001220777.1:c.446-73G>T NP_001207706.1:n.446-73G>T
NM_001220778.1:c.446-73G>T NP_001207707.1:n.446-73G>T
NM_001291549.1:c.548-73G>T NP_001278478.1:n.548-73G>T
NM_078467.2:c.446-73G>T NP_510867.1:n.446-73G>T
NM_000389.5:c.446-73G>T MANE Select NP_000380.1:n.446-73G>T
NM_001220777.2:c.446-73G>T NP_001207706.1:n.446-73G>T
NM_001220778.2:c.446-73G>T NP_001207707.1:n.446-73G>T
NM_001291549.3:c.548-73G>T NP_001278478.1:n.548-73G>T
NM_001374509.1:c.548-73G>T NP_001361438.1:n.548-73G>T
NM_001374510.1:c.485-73G>T NP_001361439.1:n.485-73G>T
NM_001374511.1:c.545-73G>T NP_001361440.1:n.545-73G>T
NM_001374512.1:c.*168G>T NP_001361441.1:n.*168G>T
NM_001374513.1:c.446-73G>T NP_001361442.1:n.446-73G>T
NM_078467.3:c.446-73G>T NP_510867.1:n.446-73G>T