Canonical Allele Identifier: CA1621453508

Gene: CDKN1A DINOL

Linked Data

• dbSNP Id: rs1761750711

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.36677956T>C , CM000668.2:g.36677956T>C	GRCh38
NC_000006.11:g.36645733T>C , CM000668.1:g.36645733T>C	GRCh37
NC_000006.10:g.36753711T>C	NCBI36
NG_009364.1:g.4275T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000448526.6:c.-6+23T>C (CDKN1A)	ENSP00000409259.3:n.-6+23T>C
ENST00000459970.1:n.189+23T>C (CDKN1A)
ENST00000615513.4:c.-6+1432T>C (CDKN1A)	ENSP00000482768.1:n.-6+1432T>C
NM_001220777.1:c.-6+1432T>C (CDKN1A)	NP_001207706.1:n.-6+1432T>C
NM_001291549.1:c.97+23T>C (CDKN1A)	NP_001278478.1:n.97+23T>C
NM_078467.2:c.-6+23T>C (CDKN1A)	NP_510867.1:n.-6+23T>C
NR_144384.1:n.604A>G (DINOL)
NM_001220777.2:c.-6+1432T>C (CDKN1A)	NP_001207706.1:n.-6+1432T>C
NM_001291549.3:c.97+23T>C (CDKN1A)	NP_001278478.1:n.97+23T>C
NM_001374509.1:c.97+23T>C (CDKN1A)	NP_001361438.1:n.97+23T>C
NM_001374510.1:c.34+1386T>C (CDKN1A)	NP_001361439.1:n.34+1386T>C
NM_078467.3:c.-6+23T>C (CDKN1A)	NP_510867.1:n.-6+23T>C