Canonical Allele Identifier: CA1839157762

Gene: CDKN2A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21968096T= , CM000671.2:g.21968096T=	GRCh38
NC_000009.11:g.21968095T= , CM000671.1:g.21968095T=	GRCh37
NC_000009.10:g.21958095T=	NCBI36
NG_007485.1:g.31396A= , LRG_11:g.31396A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000304494.10:c.*133A= MANE Select	ENSP00000307101.5:n.*133A=
ENST00000404796.3:c.348-61337T=	ENSP00000385916.2:n.348-61337T=
ENST00000579755.2:c.*248A= MANE Plus Clinical	ENSP00000462950.1:n.*248A=
ENST00000304494.9:c.*133A=	ENSP00000307101.5:n.*133A=
ENST00000361570.4:c.*133A=	ENSP00000355153.4:n.*133A=
ENST00000404796.2:c.348-61337T=	ENSP00000385916.2:n.348-61337T=
ENST00000498124.1:c.*297A=	ENSP00000418915.1:n.*297A=
ENST00000530628.2:c.*174A=	ENSP00000432664.2:n.*174A=
ENST00000578845.2:c.*133A=	ENSP00000467390.1:n.*133A=
ENST00000579122.1:c.*113A=	ENSP00000464202.1:n.*113A=
ENST00000579755.1:c.*248A=	ENSP00000462950.1:n.*248A=
NM_000077.4:c.*133A= , LRG_11t1:c.*133A=	NP_000068.1:n.*133A=
NM_001195132.1:c.*297A=	NP_001182061.1:n.*297A=
NM_058195.3:c.*248A= , LRG_11t2:c.*248A=	NP_478102.2:n.*248A=
NM_058197.4:c.878A=	NP_478104.2:n.878A=
XM_005251343.1:c.*133A=	XP_005251400.1:n.*133A=
XM_011517679.1:c.*133A=	XP_011515981.1:n.*133A=
NM_001363763.1:c.*133A=	NP_001350692.1:n.*133A=
NM_001363763.2:c.*133A=	NP_001350692.1:n.*133A=
NM_000077.5:c.*133A= MANE Select	NP_000068.1:n.*133A=
NM_001195132.2:c.*297A=	NP_001182061.1:n.*297A=
NM_058195.4:c.*248A= MANE Plus Clinical	NP_478102.2:n.*248A=
NM_058197.5:c.*527A=	NP_478104.2:n.*527A=