Canonical Allele Identifier: CA1839157769

Gene: CDKN2A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21968101A= , CM000671.2:g.21968101A=	GRCh38
NC_000009.11:g.21968100A= , CM000671.1:g.21968100A=	GRCh37
NC_000009.10:g.21958100A=	NCBI36
NG_007485.1:g.31391T= , LRG_11:g.31391T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304494.10:c.*128T= MANE Select	ENSP00000307101.5:n.*128T=
ENST00000404796.3:c.348-61332A=	ENSP00000385916.2:n.348-61332A=
ENST00000579755.2:c.*243T= MANE Plus Clinical	ENSP00000462950.1:n.*243T=
ENST00000304494.9:c.*128T=	ENSP00000307101.5:n.*128T=
ENST00000361570.4:c.*128T=	ENSP00000355153.4:n.*128T=
ENST00000404796.2:c.348-61332A=	ENSP00000385916.2:n.348-61332A=
ENST00000498124.1:c.*292T=	ENSP00000418915.1:n.*292T=
ENST00000530628.2:c.*169T=	ENSP00000432664.2:n.*169T=
ENST00000578845.2:c.*128T=	ENSP00000467390.1:n.*128T=
ENST00000579122.1:c.*108T=	ENSP00000464202.1:n.*108T=
ENST00000579755.1:c.*243T=	ENSP00000462950.1:n.*243T=
NM_000077.4:c.*128T= , LRG_11t1:c.*128T=	NP_000068.1:n.*128T=
NM_001195132.1:c.*292T=	NP_001182061.1:n.*292T=
NM_058195.3:c.*243T= , LRG_11t2:c.*243T=	NP_478102.2:n.*243T=
NM_058197.4:c.873T=	NP_478104.2:n.873T=
XM_005251343.1:c.*128T=	XP_005251400.1:n.*128T=
XM_011517679.1:c.*128T=	XP_011515981.1:n.*128T=
NM_001363763.1:c.*128T=	NP_001350692.1:n.*128T=
NM_001363763.2:c.*128T=	NP_001350692.1:n.*128T=
NM_000077.5:c.*128T= MANE Select	NP_000068.1:n.*128T=
NM_001195132.2:c.*292T=	NP_001182061.1:n.*292T=
NM_058195.4:c.*243T= MANE Plus Clinical	NP_478102.2:n.*243T=
NM_058197.5:c.*522T=	NP_478104.2:n.*522T=