Canonical Allele Identifier: CA137415981
Gene: CDKN1A HGNC NCBI
DINOL HGNC NCBI

Linked Data

dbSNP Id: rs904449821
gnomAD v3: 6-36677871-C-G
gnomAD v4: 6-36677871-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.36677871C>G , CM000668.2:g.36677871C>G GRCh38
NC_000006.11:g.36645648C>G , CM000668.1:g.36645648C>G GRCh37
NC_000006.10:g.36753626C>G NCBI36
NG_009364.1:g.4190C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000448526.6:c.-37-31C>G (CDKN1A) ENSP00000409259.3:n.-37-31C>G
ENST00000459970.1:n.127C>G (CDKN1A)
ENST00000615513.4:c.-6+1347C>G (CDKN1A) ENSP00000482768.1:n.-6+1347C>G
NM_001220777.1:c.-6+1347C>G (CDKN1A) NP_001207706.1:n.-6+1347C>G
NM_001291549.1:c.35C>G (CDKN1A) NP_001278478.1:p.Ser12Trp
NM_078467.2:c.-37-31C>G (CDKN1A) NP_510867.1:n.-37-31C>G
NR_144384.1:n.689G>C (DINOL)
NM_001220777.2:c.-6+1347C>G (CDKN1A) NP_001207706.1:n.-6+1347C>G
NM_001291549.3:c.35C>G (CDKN1A) NP_001278478.1:p.Ser12Trp
NM_001374509.1:c.35C>G (CDKN1A) NP_001361438.1:p.Ser12Trp
NM_001374510.1:c.34+1301C>G (CDKN1A) NP_001361439.1:n.34+1301C>G
NM_078467.3:c.-37-31C>G (CDKN1A) NP_510867.1:n.-37-31C>G