Canonical Allele Identifier: CA1839158034

Gene: CDKN2A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21968234C= , CM000671.2:g.21968234C=	GRCh38
NC_000009.11:g.21968233C= , CM000671.1:g.21968233C=	GRCh37
NC_000009.10:g.21958233C=	NCBI36
NG_007485.1:g.31258G= , LRG_11:g.31258G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000304494.10:c.466G= MANE Select	ENSP00000307101.5:p.Asp156=
ENST00000404796.3:c.348-61199C=	ENSP00000385916.2:n.348-61199C=
ENST00000579755.2:c.*110G= MANE Plus Clinical	ENSP00000462950.1:n.*110G=
ENST00000304494.9:c.466G=	ENSP00000307101.5:p.Asp156=
ENST00000361570.4:c.508G=	ENSP00000355153.4:p.Asp170=
ENST00000380151.3:c.740G=	ENSP00000369496.3:n.740G=
ENST00000404796.2:c.348-61199C=	ENSP00000385916.2:n.348-61199C=
ENST00000494262.5:c.313G=	ENSP00000464952.1:p.Asp105=
ENST00000498124.1:c.*159G=	ENSP00000418915.1:n.*159G=
ENST00000498628.6:c.313G=	ENSP00000467857.1:p.Asp105=
ENST00000530628.2:c.*36G=	ENSP00000432664.2:n.*36G=
ENST00000578845.2:c.313G=	ENSP00000467390.1:p.Asp105=
ENST00000579122.1:c.392G=	ENSP00000464202.1:p.Arg131=
ENST00000579755.1:c.*110G=	ENSP00000462950.1:n.*110G=
NM_000077.4:c.466G= , LRG_11t1:c.466G=	NP_000068.1:p.Asp156=
NM_001195132.1:c.*159G=	NP_001182061.1:n.*159G=
NM_058195.3:c.*110G= , LRG_11t2:c.*110G=	NP_478102.2:n.*110G=
NM_058197.4:c.740G=	NP_478104.2:n.740G=
XM_005251343.1:c.313G=	XP_005251400.1:p.Asp105=
XM_011517679.1:c.313G=	XP_011515981.1:p.Asp105=
NM_001363763.1:c.313G=	NP_001350692.1:p.Asp105=
NM_001363763.2:c.313G=	NP_001350692.1:p.Asp105=
NM_000077.5:c.466G= MANE Select	NP_000068.1:p.Asp156=
NM_001195132.2:c.*159G=	NP_001182061.1:n.*159G=
NM_058195.4:c.*110G= MANE Plus Clinical	NP_478102.2:n.*110G=
NM_058197.5:c.*389G=	NP_478104.2:n.*389G=