Canonical Allele Identifier: CA1621455076

Gene: CDKN1A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.36681067C= , CM000668.2:g.36681067C=	GRCh38
NC_000006.11:g.36648844C= , CM000668.1:g.36648844C=	GRCh37
NC_000006.10:g.36756822C=	NCBI36
NG_009364.1:g.7386C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000244741.10:c.-6+2269C= MANE Select	ENSP00000244741.6:n.-6+2269C=
ENST00000244741.9:c.-6+2269C=	ENSP00000244741.5:n.-6+2269C=
ENST00000373711.3:c.-96-1573C=	ENSP00000362815.1:n.-96-1573C=
ENST00000405375.5:c.-6+2128C=	ENSP00000384849.1:n.-6+2128C=
ENST00000448526.6:c.-5-3030C=	ENSP00000409259.3:n.-5-3030C=
ENST00000459970.1:n.190-3030C=
ENST00000478800.1:n.214+2128C=
ENST00000615513.4:c.-5-3030C=	ENSP00000482768.1:n.-5-3030C=
NM_000389.4:c.-6+2269C=	NP_000380.1:n.-6+2269C=
NM_001220777.1:c.-5-3030C=	NP_001207706.1:n.-5-3030C=
NM_001220778.1:c.-6+2128C=	NP_001207707.1:n.-6+2128C=
NM_001291549.1:c.98-3030C=	NP_001278478.1:n.98-3030C=
NM_078467.2:c.-5-3030C=	NP_510867.1:n.-5-3030C=
XM_011515041.1:c.*213C=	XP_011513343.1:n.*213C=
NM_000389.5:c.-6+2269C= MANE Select	NP_000380.1:n.-6+2269C=
NM_001220777.2:c.-5-3030C=	NP_001207706.1:n.-5-3030C=
NM_001220778.2:c.-6+2128C=	NP_001207707.1:n.-6+2128C=
NM_001291549.3:c.98-3030C=	NP_001278478.1:n.98-3030C=
NM_001374509.1:c.98-3030C=	NP_001361438.1:n.98-3030C=
NM_001374510.1:c.35-3030C=	NP_001361439.1:n.35-3030C=
NM_001374511.1:c.-6+2269C=	NP_001361440.1:n.-6+2269C=
NM_001374512.1:c.-6+2269C=	NP_001361441.1:n.-6+2269C=
NM_001374513.1:c.-6+2162C=	NP_001361442.1:n.-6+2162C=
NM_078467.3:c.-5-3030C=	NP_510867.1:n.-5-3030C=