Canonical Allele Identifier: CA1839158021

Gene: CDKN2A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21968229T= , CM000671.2:g.21968229T=	GRCh38
NC_000009.11:g.21968228T= , CM000671.1:g.21968228T=	GRCh37
NC_000009.10:g.21958228T=	NCBI36
NG_007485.1:g.31263A= , LRG_11:g.31263A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304494.10:c.471A= MANE Select	ENSP00000307101.5:p.Ter157=
ENST00000404796.3:c.348-61204T=	ENSP00000385916.2:n.348-61204T=
ENST00000579755.2:c.*115A= MANE Plus Clinical	ENSP00000462950.1:n.*115A=
ENST00000304494.9:c.471A=	ENSP00000307101.5:p.Ter157=
ENST00000361570.4:c.513A=	ENSP00000355153.4:p.Ter171=
ENST00000380151.3:c.745A=	ENSP00000369496.3:n.745A=
ENST00000404796.2:c.348-61204T=	ENSP00000385916.2:n.348-61204T=
ENST00000494262.5:c.318A=	ENSP00000464952.1:p.Ter106=
ENST00000498124.1:c.*164A=	ENSP00000418915.1:n.*164A=
ENST00000498628.6:c.318A=	ENSP00000467857.1:p.Ter106=
ENST00000530628.2:c.*41A=	ENSP00000432664.2:n.*41A=
ENST00000578845.2:c.318A=	ENSP00000467390.1:p.Ter106=
ENST00000579122.1:c.397A=	ENSP00000464202.1:p.Lys133=
ENST00000579755.1:c.*115A=	ENSP00000462950.1:n.*115A=
NM_000077.4:c.471A= , LRG_11t1:c.471A=	NP_000068.1:p.Ter157=
NM_001195132.1:c.*164A=	NP_001182061.1:n.*164A=
NM_058195.3:c.*115A= , LRG_11t2:c.*115A=	NP_478102.2:n.*115A=
NM_058197.4:c.745A=	NP_478104.2:n.745A=
XM_005251343.1:c.318A=	XP_005251400.1:p.Ter106=
XM_011517679.1:c.318A=	XP_011515981.1:p.Ter106=
NM_001363763.1:c.318A=	NP_001350692.1:p.Ter106=
NM_001363763.2:c.318A=	NP_001350692.1:p.Ter106=
NM_000077.5:c.471A= MANE Select	NP_000068.1:p.Ter157=
NM_001195132.2:c.*164A=	NP_001182061.1:n.*164A=
NM_058195.4:c.*115A= MANE Plus Clinical	NP_478102.2:n.*115A=
NM_058197.5:c.*394A=	NP_478104.2:n.*394A=