Canonical Allele Identifier: CA1621455010

Gene: CDKN1A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.36680868G= , CM000668.2:g.36680868G=	GRCh38
NC_000006.11:g.36648645G= , CM000668.1:g.36648645G=	GRCh37
NC_000006.10:g.36756623G=	NCBI36
NG_009364.1:g.7187G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000244741.10:c.-6+2070G= MANE Select	ENSP00000244741.6:n.-6+2070G=
ENST00000244741.9:c.-6+2070G=	ENSP00000244741.5:n.-6+2070G=
ENST00000373711.3:c.-96-1772G=	ENSP00000362815.1:n.-96-1772G=
ENST00000405375.5:c.-6+1929G=	ENSP00000384849.1:n.-6+1929G=
ENST00000448526.6:c.-6+2935G=	ENSP00000409259.3:n.-6+2935G=
ENST00000459970.1:n.189+2935G=
ENST00000478800.1:n.214+1929G=
ENST00000615513.4:c.-5-3229G=	ENSP00000482768.1:n.-5-3229G=
NM_000389.4:c.-6+2070G=	NP_000380.1:n.-6+2070G=
NM_001220777.1:c.-5-3229G=	NP_001207706.1:n.-5-3229G=
NM_001220778.1:c.-6+1929G=	NP_001207707.1:n.-6+1929G=
NM_001291549.1:c.97+2935G=	NP_001278478.1:n.97+2935G=
NM_078467.2:c.-6+2935G=	NP_510867.1:n.-6+2935G=
XM_011515041.1:c.*14G=	XP_011513343.1:n.*14G=
NM_000389.5:c.-6+2070G= MANE Select	NP_000380.1:n.-6+2070G=
NM_001220777.2:c.-5-3229G=	NP_001207706.1:n.-5-3229G=
NM_001220778.2:c.-6+1929G=	NP_001207707.1:n.-6+1929G=
NM_001291549.3:c.97+2935G=	NP_001278478.1:n.97+2935G=
NM_001374509.1:c.97+2935G=	NP_001361438.1:n.97+2935G=
NM_001374510.1:c.35-3229G=	NP_001361439.1:n.35-3229G=
NM_001374511.1:c.-6+2070G=	NP_001361440.1:n.-6+2070G=
NM_001374512.1:c.-6+2070G=	NP_001361441.1:n.-6+2070G=
NM_001374513.1:c.-6+1963G=	NP_001361442.1:n.-6+1963G=
NM_078467.3:c.-6+2935G=	NP_510867.1:n.-6+2935G=