Canonical Allele Identifier: CA566530367
Gene: CDKN1A HGNC NCBI
DINOL HGNC NCBI

Linked Data

dbSNP Id: rs1197955056
gnomAD v2: 6-36645700-C-T
gnomAD v4: 6-36677923-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.36677923C>T , CM000668.2:g.36677923C>T GRCh38
NC_000006.11:g.36645700C>T , CM000668.1:g.36645700C>T GRCh37
NC_000006.10:g.36753678C>T NCBI36
NG_009364.1:g.4242C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000448526.6:c.-16C>T (CDKN1A) ENSP00000409259.3:n.-16C>T
ENST00000459970.1:n.179C>T (CDKN1A)
ENST00000615513.4:c.-6+1399C>T (CDKN1A) ENSP00000482768.1:n.-6+1399C>T
NM_001220777.1:c.-6+1399C>T (CDKN1A) NP_001207706.1:n.-6+1399C>T
NM_001291549.1:c.87C>T (CDKN1A) NP_001278478.1:p.Phe29=
NM_078467.2:c.-16C>T (CDKN1A) NP_510867.1:n.-16C>T
NR_144384.1:n.637G>A (DINOL)
NM_001220777.2:c.-6+1399C>T (CDKN1A) NP_001207706.1:n.-6+1399C>T
NM_001291549.3:c.87C>T (CDKN1A) NP_001278478.1:p.Phe29=
NM_001374509.1:c.87C>T (CDKN1A) NP_001361438.1:p.Phe29=
NM_001374510.1:c.34+1353C>T (CDKN1A) NP_001361439.1:n.34+1353C>T
NM_078467.3:c.-16C>T (CDKN1A) NP_510867.1:n.-16C>T