Canonical Allele Identifier: CA363834825

Gene: CDKN1A

Linked Data

• MyVariant Identifiers: chr6:g.36653567G>T (hg19) ; chr6:g.36685790G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.36685790G>T , CM000668.2:g.36685790G>T	GRCh38
NC_000006.11:g.36653567G>T , CM000668.1:g.36653567G>T	GRCh37
NC_000006.10:g.36761545G>T	NCBI36
NG_009364.1:g.12109G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000244741.10:c.485G>T MANE Select	ENSP00000244741.6:p.Arg162Met
ENST00000244741.9:c.485G>T	ENSP00000244741.5:p.Arg162Met
ENST00000373711.3:c.485G>T	ENSP00000362815.1:p.Arg162Met
ENST00000405375.5:c.485G>T	ENSP00000384849.1:p.Arg162Met
ENST00000448526.6:c.485G>T	ENSP00000409259.3:p.Arg162Met
ENST00000615513.4:c.485G>T	ENSP00000482768.1:p.Arg162Met
NM_000389.4:c.485G>T	NP_000380.1:p.Arg162Met
NM_001220777.1:c.485G>T	NP_001207706.1:p.Arg162Met
NM_001220778.1:c.485G>T	NP_001207707.1:p.Arg162Met
NM_001291549.1:c.587G>T	NP_001278478.1:p.Arg196Met
NM_078467.2:c.485G>T	NP_510867.1:p.Arg162Met
NM_000389.5:c.485G>T MANE Select	NP_000380.1:p.Arg162Met
NM_001220777.2:c.485G>T	NP_001207706.1:p.Arg162Met
NM_001220778.2:c.485G>T	NP_001207707.1:p.Arg162Met
NM_001291549.3:c.587G>T	NP_001278478.1:p.Arg196Met
NM_001374509.1:c.587G>T	NP_001361438.1:p.Arg196Met
NM_001374510.1:c.524G>T	NP_001361439.1:p.Arg175Met
NM_001374511.1:c.584G>T	NP_001361440.1:p.Arg195Met
NM_001374512.1:c.*280G>T	NP_001361441.1:n.*280G>T
NM_001374513.1:c.485G>T	NP_001361442.1:p.Arg162Met
NM_078467.3:c.485G>T	NP_510867.1:p.Arg162Met