Canonical Allele Identifier: CA1839158038

Gene: CDKN2A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21968235G= , CM000671.2:g.21968235G=	GRCh38
NC_000009.11:g.21968234G= , CM000671.1:g.21968234G=	GRCh37
NC_000009.10:g.21958234G=	NCBI36
NG_007485.1:g.31257C= , LRG_11:g.31257C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000304494.10:c.465C= MANE Select	ENSP00000307101.5:p.Pro155=
ENST00000404796.3:c.348-61198G=	ENSP00000385916.2:n.348-61198G=
ENST00000579755.2:c.*109C= MANE Plus Clinical	ENSP00000462950.1:n.*109C=
ENST00000304494.9:c.465C=	ENSP00000307101.5:p.Pro155=
ENST00000361570.4:c.507C=	ENSP00000355153.4:p.Pro169=
ENST00000380151.3:c.739C=	ENSP00000369496.3:n.739C=
ENST00000404796.2:c.348-61198G=	ENSP00000385916.2:n.348-61198G=
ENST00000494262.5:c.312C=	ENSP00000464952.1:p.Pro104=
ENST00000498124.1:c.*158C=	ENSP00000418915.1:n.*158C=
ENST00000498628.6:c.312C=	ENSP00000467857.1:p.Pro104=
ENST00000530628.2:c.*35C=	ENSP00000432664.2:n.*35C=
ENST00000578845.2:c.312C=	ENSP00000467390.1:p.Pro104=
ENST00000579122.1:c.391C=	ENSP00000464202.1:p.Arg131=
ENST00000579755.1:c.*109C=	ENSP00000462950.1:n.*109C=
NM_000077.4:c.465C= , LRG_11t1:c.465C=	NP_000068.1:p.Pro155=
NM_001195132.1:c.*158C=	NP_001182061.1:n.*158C=
NM_058195.3:c.*109C= , LRG_11t2:c.*109C=	NP_478102.2:n.*109C=
NM_058197.4:c.739C=	NP_478104.2:n.739C=
XM_005251343.1:c.312C=	XP_005251400.1:p.Pro104=
XM_011517679.1:c.312C=	XP_011515981.1:p.Pro104=
NM_001363763.1:c.312C=	NP_001350692.1:p.Pro104=
NM_001363763.2:c.312C=	NP_001350692.1:p.Pro104=
NM_000077.5:c.465C= MANE Select	NP_000068.1:p.Pro155=
NM_001195132.2:c.*158C=	NP_001182061.1:n.*158C=
NM_058195.4:c.*109C= MANE Plus Clinical	NP_478102.2:n.*109C=
NM_058197.5:c.*388C=	NP_478104.2:n.*388C=