Canonical Allele Identifier: CA1839157681

Gene: CDKN2A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21968025A= , CM000671.2:g.21968025A=	GRCh38
NC_000009.11:g.21968024A= , CM000671.1:g.21968024A=	GRCh37
NC_000009.10:g.21958024A=	NCBI36
NG_007485.1:g.31467T= , LRG_11:g.31467T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000304494.10:c.*204T= MANE Select	ENSP00000307101.5:n.*204T=
ENST00000404796.3:c.348-61408A=	ENSP00000385916.2:n.348-61408A=
ENST00000579755.2:c.*319T= MANE Plus Clinical	ENSP00000462950.1:n.*319T=
ENST00000304494.9:c.*204T=	ENSP00000307101.5:n.*204T=
ENST00000361570.4:c.*204T=	ENSP00000355153.4:n.*204T=
ENST00000404796.2:c.348-61408A=	ENSP00000385916.2:n.348-61408A=
ENST00000530628.2:c.*245T=	ENSP00000432664.2:n.*245T=
ENST00000578845.2:c.*204T=	ENSP00000467390.1:n.*204T=
ENST00000579122.1:c.*184T=	ENSP00000464202.1:n.*184T=
ENST00000579755.1:c.*319T=	ENSP00000462950.1:n.*319T=
NM_000077.4:c.*204T= , LRG_11t1:c.*204T=	NP_000068.1:n.*204T=
NM_001195132.1:c.*368T=	NP_001182061.1:n.*368T=
NM_058195.3:c.*319T= , LRG_11t2:c.*319T=	NP_478102.2:n.*319T=
NM_058197.4:c.949T=	NP_478104.2:n.949T=
XM_005251343.1:c.*204T=	XP_005251400.1:n.*204T=
XM_011517679.1:c.*204T=	XP_011515981.1:n.*204T=
NM_001363763.1:c.*204T=	NP_001350692.1:n.*204T=
NM_001363763.2:c.*204T=	NP_001350692.1:n.*204T=
NM_000077.5:c.*204T= MANE Select	NP_000068.1:n.*204T=
NM_001195132.2:c.*368T=	NP_001182061.1:n.*368T=
NM_058195.4:c.*319T= MANE Plus Clinical	NP_478102.2:n.*319T=
NM_058197.5:c.*598T=	NP_478104.2:n.*598T=