Canonical Allele Identifier: CA449976577

Gene: CDKN1A

Linked Data

• gnomAD v4: 6-36685799-A-G
• MyVariant Identifiers: chr6:g.36653576A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.36685799A>G , CM000668.2:g.36685799A>G	GRCh38
NC_000006.11:g.36653576A>G , CM000668.1:g.36653576A>G	GRCh37
NC_000006.10:g.36761554A>G	NCBI36
NG_009364.1:g.12118A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000244741.10:c.494A>G MANE Select	ENSP00000244741.6:p.Ter165=
ENST00000244741.9:c.494A>G	ENSP00000244741.5:p.Ter165=
ENST00000373711.3:c.494A>G	ENSP00000362815.1:p.Ter165=
ENST00000405375.5:c.494A>G	ENSP00000384849.1:p.Ter165=
ENST00000448526.6:c.494A>G	ENSP00000409259.3:p.Ter165=
ENST00000615513.4:c.494A>G	ENSP00000482768.1:p.Ter165=
NM_000389.4:c.494A>G	NP_000380.1:p.Ter165=
NM_001220777.1:c.494A>G	NP_001207706.1:p.Ter165=
NM_001220778.1:c.494A>G	NP_001207707.1:p.Ter165=
NM_001291549.1:c.596A>G	NP_001278478.1:p.Ter199=
NM_078467.2:c.494A>G	NP_510867.1:p.Ter165=
NM_000389.5:c.494A>G MANE Select	NP_000380.1:p.Ter165=
NM_001220777.2:c.494A>G	NP_001207706.1:p.Ter165=
NM_001220778.2:c.494A>G	NP_001207707.1:p.Ter165=
NM_001291549.3:c.596A>G	NP_001278478.1:p.Ter199=
NM_001374509.1:c.596A>G	NP_001361438.1:p.Ter199=
NM_001374510.1:c.533A>G	NP_001361439.1:p.Ter178=
NM_001374511.1:c.593A>G	NP_001361440.1:p.Ter198=
NM_001374512.1:c.*289A>G	NP_001361441.1:n.*289A>G
NM_001374513.1:c.494A>G	NP_001361442.1:p.Ter165=
NM_078467.3:c.494A>G	NP_510867.1:p.Ter165=