Canonical Allele Identifier: CA3780452

Gene: CDKN1A

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.36685832C>T , CM000668.2:g.36685832C>T	GRCh38
NC_000006.11:g.36653609C>T , CM000668.1:g.36653609C>T	GRCh37
NC_000006.10:g.36761587C>T	NCBI36
NG_009364.1:g.12151C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000244741.10:c.*32C>T MANE Select	ENSP00000244741.6:n.*32C>T
ENST00000244741.9:c.*32C>T	ENSP00000244741.5:n.*32C>T
ENST00000373711.3:c.*32C>T	ENSP00000362815.1:n.*32C>T
ENST00000405375.5:c.*32C>T	ENSP00000384849.1:n.*32C>T
ENST00000448526.6:c.*32C>T	ENSP00000409259.3:n.*32C>T
ENST00000615513.4:c.*32C>T	ENSP00000482768.1:n.*32C>T
NM_000389.4:c.*32C>T	NP_000380.1:n.*32C>T
NM_001220777.1:c.*32C>T	NP_001207706.1:n.*32C>T
NM_001220778.1:c.*32C>T	NP_001207707.1:n.*32C>T
NM_001291549.1:c.*32C>T	NP_001278478.1:n.*32C>T
NM_078467.2:c.*32C>T	NP_510867.1:n.*32C>T
NM_000389.5:c.*32C>T MANE Select	NP_000380.1:n.*32C>T
NM_001220777.2:c.*32C>T	NP_001207706.1:n.*32C>T
NM_001220778.2:c.*32C>T	NP_001207707.1:n.*32C>T
NM_001291549.3:c.*32C>T	NP_001278478.1:n.*32C>T
NM_001374509.1:c.*32C>T	NP_001361438.1:n.*32C>T
NM_001374510.1:c.*32C>T	NP_001361439.1:n.*32C>T
NM_001374511.1:c.*32C>T	NP_001361440.1:n.*32C>T
NM_001374512.1:c.*322C>T	NP_001361441.1:n.*322C>T
NM_001374513.1:c.*32C>T	NP_001361442.1:n.*32C>T
NM_078467.3:c.*32C>T	NP_510867.1:n.*32C>T