Canonical Allele Identifier: CA566530375

Gene: CDKN1A DINOL

Linked Data

• dbSNP Id: rs1362077569
• gnomAD v2: 6-36645722-G-T
• gnomAD v4: 6-36677945-G-T
• MyVariant Identifiers: chr6:g.36645722G>T (hg19) ; chr6:g.36677945G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.36677945G>T , CM000668.2:g.36677945G>T	GRCh38
NC_000006.11:g.36645722G>T , CM000668.1:g.36645722G>T	GRCh37
NC_000006.10:g.36753700G>T	NCBI36
NG_009364.1:g.4264G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000448526.6:c.-6+12G>T (CDKN1A)	ENSP00000409259.3:n.-6+12G>T
ENST00000459970.1:n.189+12G>T (CDKN1A)
ENST00000615513.4:c.-6+1421G>T (CDKN1A)	ENSP00000482768.1:n.-6+1421G>T
NM_001220777.1:c.-6+1421G>T (CDKN1A)	NP_001207706.1:n.-6+1421G>T
NM_001291549.1:c.97+12G>T (CDKN1A)	NP_001278478.1:n.97+12G>T
NM_078467.2:c.-6+12G>T (CDKN1A)	NP_510867.1:n.-6+12G>T
NR_144384.1:n.615C>A (DINOL)
NM_001220777.2:c.-6+1421G>T (CDKN1A)	NP_001207706.1:n.-6+1421G>T
NM_001291549.3:c.97+12G>T (CDKN1A)	NP_001278478.1:n.97+12G>T
NM_001374509.1:c.97+12G>T (CDKN1A)	NP_001361438.1:n.97+12G>T
NM_001374510.1:c.34+1375G>T (CDKN1A)	NP_001361439.1:n.34+1375G>T
NM_078467.3:c.-6+12G>T (CDKN1A)	NP_510867.1:n.-6+12G>T