Canonical Allele Identifier: CA1621453386
Gene: CDKN1A HGNC NCBI
DINOL HGNC NCBI

Linked Data

dbSNP Id: rs1761738631
gnomAD v4: 6-36677673-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.36677673T>C , CM000668.2:g.36677673T>C GRCh38
NC_000006.11:g.36645450T>C , CM000668.1:g.36645450T>C GRCh37
NC_000006.10:g.36753428T>C NCBI36
NG_009364.1:g.3992T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000448526.6:c.-37-229T>C (CDKN1A) ENSP00000409259.3:n.-37-229T>C
ENST00000459970.1:n.44-115T>C (CDKN1A)
ENST00000615513.4:c.-6+1149T>C (CDKN1A) ENSP00000482768.1:n.-6+1149T>C
NM_001220777.1:c.-6+1149T>C (CDKN1A) NP_001207706.1:n.-6+1149T>C
NM_001291549.1:c.-141-23T>C (CDKN1A) NP_001278478.1:n.-141-23T>C
NM_078467.2:c.-37-229T>C (CDKN1A) NP_510867.1:n.-37-229T>C
NR_144384.1:n.887A>G (DINOL)
NM_001220777.2:c.-6+1149T>C (CDKN1A) NP_001207706.1:n.-6+1149T>C
NM_001291549.3:c.-141-23T>C (CDKN1A) NP_001278478.1:n.-141-23T>C
NM_001374509.1:c.-49-115T>C (CDKN1A) NP_001361438.1:n.-49-115T>C
NM_001374510.1:c.34+1103T>C (CDKN1A) NP_001361439.1:n.34+1103T>C
NM_078467.3:c.-37-229T>C (CDKN1A) NP_510867.1:n.-37-229T>C