Canonical Allele Identifier: CA137416083

Gene: CDKN1A DINOL

Linked Data

• dbSNP Id: rs761892356
• gnomAD v4: 6-36677941-T-A
• MyVariant Identifiers: chr6:g.36645718T>A (hg19) ; chr6:g.36677941T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.36677941T>A , CM000668.2:g.36677941T>A	GRCh38
NC_000006.11:g.36645718T>A , CM000668.1:g.36645718T>A	GRCh37
NC_000006.10:g.36753696T>A	NCBI36
NG_009364.1:g.4260T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000448526.6:c.-6+8T>A (CDKN1A)	ENSP00000409259.3:n.-6+8T>A
ENST00000459970.1:n.189+8T>A (CDKN1A)
ENST00000615513.4:c.-6+1417T>A (CDKN1A)	ENSP00000482768.1:n.-6+1417T>A
NM_001220777.1:c.-6+1417T>A (CDKN1A)	NP_001207706.1:n.-6+1417T>A
NM_001291549.1:c.97+8T>A (CDKN1A)	NP_001278478.1:n.97+8T>A
NM_078467.2:c.-6+8T>A (CDKN1A)	NP_510867.1:n.-6+8T>A
NR_144384.1:n.619A>T (DINOL)
NM_001220777.2:c.-6+1417T>A (CDKN1A)	NP_001207706.1:n.-6+1417T>A
NM_001291549.3:c.97+8T>A (CDKN1A)	NP_001278478.1:n.97+8T>A
NM_001374509.1:c.97+8T>A (CDKN1A)	NP_001361438.1:n.97+8T>A
NM_001374510.1:c.34+1371T>A (CDKN1A)	NP_001361439.1:n.34+1371T>A
NM_078467.3:c.-6+8T>A (CDKN1A)	NP_510867.1:n.-6+8T>A