Canonical Allele Identifier: CA137424890

Gene: CDKN1A

Linked Data

• dbSNP Id: rs770267002
• gnomAD v2: 6-36653598-A-C
• gnomAD v4: 6-36685821-A-C
• MyVariant Identifiers: chr6:g.36653598A>C (hg19) ; chr6:g.36685821A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.36685821A>C , CM000668.2:g.36685821A>C	GRCh38
NC_000006.11:g.36653598A>C , CM000668.1:g.36653598A>C	GRCh37
NC_000006.10:g.36761576A>C	NCBI36
NG_009364.1:g.12140A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000244741.10:c.*21A>C MANE Select	ENSP00000244741.6:n.*21A>C
ENST00000244741.9:c.*21A>C	ENSP00000244741.5:n.*21A>C
ENST00000373711.3:c.*21A>C	ENSP00000362815.1:n.*21A>C
ENST00000405375.5:c.*21A>C	ENSP00000384849.1:n.*21A>C
ENST00000448526.6:c.*21A>C	ENSP00000409259.3:n.*21A>C
ENST00000615513.4:c.*21A>C	ENSP00000482768.1:n.*21A>C
NM_000389.4:c.*21A>C	NP_000380.1:n.*21A>C
NM_001220777.1:c.*21A>C	NP_001207706.1:n.*21A>C
NM_001220778.1:c.*21A>C	NP_001207707.1:n.*21A>C
NM_001291549.1:c.*21A>C	NP_001278478.1:n.*21A>C
NM_078467.2:c.*21A>C	NP_510867.1:n.*21A>C
NM_000389.5:c.*21A>C MANE Select	NP_000380.1:n.*21A>C
NM_001220777.2:c.*21A>C	NP_001207706.1:n.*21A>C
NM_001220778.2:c.*21A>C	NP_001207707.1:n.*21A>C
NM_001291549.3:c.*21A>C	NP_001278478.1:n.*21A>C
NM_001374509.1:c.*21A>C	NP_001361438.1:n.*21A>C
NM_001374510.1:c.*21A>C	NP_001361439.1:n.*21A>C
NM_001374511.1:c.*21A>C	NP_001361440.1:n.*21A>C
NM_001374512.1:c.*311A>C	NP_001361441.1:n.*311A>C
NM_001374513.1:c.*21A>C	NP_001361442.1:n.*21A>C
NM_078467.3:c.*21A>C	NP_510867.1:n.*21A>C