Canonical Allele Identifier: CA566530378
Gene: CDKN1A HGNC NCBI
DINOL HGNC NCBI

Linked Data

dbSNP Id: rs1360983719
gnomAD v2: 6-36645730-A-T
gnomAD v3: 6-36677953-A-T
gnomAD v4: 6-36677953-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.36677953A>T , CM000668.2:g.36677953A>T GRCh38
NC_000006.11:g.36645730A>T , CM000668.1:g.36645730A>T GRCh37
NC_000006.10:g.36753708A>T NCBI36
NG_009364.1:g.4272A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000448526.6:c.-6+20A>T (CDKN1A) ENSP00000409259.3:n.-6+20A>T
ENST00000459970.1:n.189+20A>T (CDKN1A)
ENST00000615513.4:c.-6+1429A>T (CDKN1A) ENSP00000482768.1:n.-6+1429A>T
NM_001220777.1:c.-6+1429A>T (CDKN1A) NP_001207706.1:n.-6+1429A>T
NM_001291549.1:c.97+20A>T (CDKN1A) NP_001278478.1:n.97+20A>T
NM_078467.2:c.-6+20A>T (CDKN1A) NP_510867.1:n.-6+20A>T
NR_144384.1:n.607T>A (DINOL)
NM_001220777.2:c.-6+1429A>T (CDKN1A) NP_001207706.1:n.-6+1429A>T
NM_001291549.3:c.97+20A>T (CDKN1A) NP_001278478.1:n.97+20A>T
NM_001374509.1:c.97+20A>T (CDKN1A) NP_001361438.1:n.97+20A>T
NM_001374510.1:c.34+1383A>T (CDKN1A) NP_001361439.1:n.34+1383A>T
NM_078467.3:c.-6+20A>T (CDKN1A) NP_510867.1:n.-6+20A>T