Canonical Allele Identifier: CA449975932

Gene: CDKN1A

Linked Data

• dbSNP Id: rs1478717705
• gnomAD v4: 6-36684197-C-A
• MyVariant Identifiers: chr6:g.36651974C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.36684197C>A , CM000668.2:g.36684197C>A	GRCh38
NC_000006.11:g.36651974C>A , CM000668.1:g.36651974C>A	GRCh37
NC_000006.10:g.36759952C>A	NCBI36
NG_009364.1:g.10516C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000244741.10:c.96C>A MANE Select	ENSP00000244741.6:p.Arg32=
ENST00000244741.9:c.96C>A	ENSP00000244741.5:p.Arg32=
ENST00000373711.3:c.96C>A	ENSP00000362815.1:p.Arg32=
ENST00000405375.5:c.96C>A	ENSP00000384849.1:p.Arg32=
ENST00000448526.6:c.96C>A	ENSP00000409259.3:p.Arg32=
ENST00000459970.1:n.290C>A
ENST00000478800.1:n.315C>A
ENST00000615513.4:c.96C>A	ENSP00000482768.1:p.Arg32=
NM_000389.4:c.96C>A	NP_000380.1:p.Arg32=
NM_001220777.1:c.96C>A	NP_001207706.1:p.Arg32=
NM_001220778.1:c.96C>A	NP_001207707.1:p.Arg32=
NM_001291549.1:c.198C>A	NP_001278478.1:p.Arg66=
NM_078467.2:c.96C>A	NP_510867.1:p.Arg32=
NM_000389.5:c.96C>A MANE Select	NP_000380.1:p.Arg32=
NM_001220777.2:c.96C>A	NP_001207706.1:p.Arg32=
NM_001220778.2:c.96C>A	NP_001207707.1:p.Arg32=
NM_001291549.3:c.198C>A	NP_001278478.1:p.Arg66=
NM_001374509.1:c.198C>A	NP_001361438.1:p.Arg66=
NM_001374510.1:c.135C>A	NP_001361439.1:p.Arg45=
NM_001374511.1:c.96C>A	NP_001361440.1:p.Arg32=
NM_001374512.1:c.96C>A	NP_001361441.1:p.Arg32=
NM_001374513.1:c.96C>A	NP_001361442.1:p.Arg32=
NM_078467.3:c.96C>A	NP_510867.1:p.Arg32=