Canonical Allele Identifier: CA1839157618

Gene: CDKN2A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21967963C= , CM000671.2:g.21967963C=	GRCh38
NC_000009.11:g.21967962C= , CM000671.1:g.21967962C=	GRCh37
NC_000009.10:g.21957962C=	NCBI36
NG_007485.1:g.31529G= , LRG_11:g.31529G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304494.10:c.*266G= MANE Select	ENSP00000307101.5:n.*266G=
ENST00000404796.3:c.348-61470C=	ENSP00000385916.2:n.348-61470C=
ENST00000579755.2:c.*381G= MANE Plus Clinical	ENSP00000462950.1:n.*381G=
ENST00000304494.9:c.*266G=	ENSP00000307101.5:n.*266G=
ENST00000361570.4:c.*266G=	ENSP00000355153.4:n.*266G=
ENST00000404796.2:c.348-61470C=	ENSP00000385916.2:n.348-61470C=
ENST00000579755.1:c.*381G=	ENSP00000462950.1:n.*381G=
NM_000077.4:c.*266G= , LRG_11t1:c.*266G=	NP_000068.1:n.*266G=
NM_001195132.1:c.*430G=	NP_001182061.1:n.*430G=
NM_058195.3:c.*381G= , LRG_11t2:c.*381G=	NP_478102.2:n.*381G=
NM_058197.4:c.1011G=	NP_478104.2:n.1011G=
XM_005251343.1:c.*266G=	XP_005251400.1:n.*266G=
XM_011517679.1:c.*266G=	XP_011515981.1:n.*266G=
NM_001363763.1:c.*266G=	NP_001350692.1:n.*266G=
NM_001363763.2:c.*266G=	NP_001350692.1:n.*266G=
NM_000077.5:c.*266G= MANE Select	NP_000068.1:n.*266G=
NM_001195132.2:c.*430G=	NP_001182061.1:n.*430G=
NM_058195.4:c.*381G= MANE Plus Clinical	NP_478102.2:n.*381G=
NM_058197.5:c.*660G=	NP_478104.2:n.*660G=