Canonical Allele Identifier: CA1621457622

Gene: CDKN1A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.36685858C= , CM000668.2:g.36685858C=	GRCh38
NC_000006.11:g.36653635C= , CM000668.1:g.36653635C=	GRCh37
NC_000006.10:g.36761613C=	NCBI36
NG_009364.1:g.12177C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000244741.10:c.*58C= MANE Select	ENSP00000244741.6:n.*58C=
ENST00000244741.9:c.*58C=	ENSP00000244741.5:n.*58C=
ENST00000373711.3:c.*58C=	ENSP00000362815.1:n.*58C=
ENST00000405375.5:c.*58C=	ENSP00000384849.1:n.*58C=
ENST00000448526.6:c.*58C=	ENSP00000409259.3:n.*58C=
ENST00000615513.4:c.*58C=	ENSP00000482768.1:n.*58C=
NM_000389.4:c.*58C=	NP_000380.1:n.*58C=
NM_001220777.1:c.*58C=	NP_001207706.1:n.*58C=
NM_001220778.1:c.*58C=	NP_001207707.1:n.*58C=
NM_001291549.1:c.*58C=	NP_001278478.1:n.*58C=
NM_078467.2:c.*58C=	NP_510867.1:n.*58C=
NM_000389.5:c.*58C= MANE Select	NP_000380.1:n.*58C=
NM_001220777.2:c.*58C=	NP_001207706.1:n.*58C=
NM_001220778.2:c.*58C=	NP_001207707.1:n.*58C=
NM_001291549.3:c.*58C=	NP_001278478.1:n.*58C=
NM_001374509.1:c.*58C=	NP_001361438.1:n.*58C=
NM_001374510.1:c.*58C=	NP_001361439.1:n.*58C=
NM_001374511.1:c.*58C=	NP_001361440.1:n.*58C=
NM_001374512.1:c.*348C=	NP_001361441.1:n.*348C=
NM_001374513.1:c.*58C=	NP_001361442.1:n.*58C=
NM_078467.3:c.*58C=	NP_510867.1:n.*58C=