Canonical Allele Identifier: CA1621453488
Gene: CDKN1A HGNC NCBI
DINOL HGNC NCBI

Linked Data

dbSNP Id: rs1264435366

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.36677918G>T , CM000668.2:g.36677918G>T GRCh38
NC_000006.11:g.36645695G>T , CM000668.1:g.36645695G>T GRCh37
NC_000006.10:g.36753673G>T NCBI36
NG_009364.1:g.4237G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000448526.6:c.-21G>T (CDKN1A) ENSP00000409259.3:n.-21G>T
ENST00000459970.1:n.174G>T (CDKN1A)
ENST00000615513.4:c.-6+1394G>T (CDKN1A) ENSP00000482768.1:n.-6+1394G>T
NM_001220777.1:c.-6+1394G>T (CDKN1A) NP_001207706.1:n.-6+1394G>T
NM_001291549.1:c.82G>T (CDKN1A) NP_001278478.1:p.Asp28Tyr
NM_078467.2:c.-21G>T (CDKN1A) NP_510867.1:n.-21G>T
NR_144384.1:n.642C>A (DINOL)
NM_001220777.2:c.-6+1394G>T (CDKN1A) NP_001207706.1:n.-6+1394G>T
NM_001291549.3:c.82G>T (CDKN1A) NP_001278478.1:p.Asp28Tyr
NM_001374509.1:c.82G>T (CDKN1A) NP_001361438.1:p.Asp28Tyr
NM_001374510.1:c.34+1348G>T (CDKN1A) NP_001361439.1:n.34+1348G>T
NM_078467.3:c.-21G>T (CDKN1A) NP_510867.1:n.-21G>T