Canonical Allele Identifier: CA1839158028

Gene: CDKN2A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21968232A= , CM000671.2:g.21968232A=	GRCh38
NC_000009.11:g.21968231A= , CM000671.1:g.21968231A=	GRCh37
NC_000009.10:g.21958231A=	NCBI36
NG_007485.1:g.31260T= , LRG_11:g.31260T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000304494.10:c.468T= MANE Select	ENSP00000307101.5:p.Asp156=
ENST00000404796.3:c.348-61201A=	ENSP00000385916.2:n.348-61201A=
ENST00000579755.2:c.*112T= MANE Plus Clinical	ENSP00000462950.1:n.*112T=
ENST00000304494.9:c.468T=	ENSP00000307101.5:p.Asp156=
ENST00000361570.4:c.510T=	ENSP00000355153.4:p.Asp170=
ENST00000380151.3:c.742T=	ENSP00000369496.3:n.742T=
ENST00000404796.2:c.348-61201A=	ENSP00000385916.2:n.348-61201A=
ENST00000494262.5:c.315T=	ENSP00000464952.1:p.Asp105=
ENST00000498124.1:c.*161T=	ENSP00000418915.1:n.*161T=
ENST00000498628.6:c.315T=	ENSP00000467857.1:p.Asp105=
ENST00000530628.2:c.*38T=	ENSP00000432664.2:n.*38T=
ENST00000578845.2:c.315T=	ENSP00000467390.1:p.Asp105=
ENST00000579122.1:c.394T=	ENSP00000464202.1:p.Leu132=
ENST00000579755.1:c.*112T=	ENSP00000462950.1:n.*112T=
NM_000077.4:c.468T= , LRG_11t1:c.468T=	NP_000068.1:p.Asp156=
NM_001195132.1:c.*161T=	NP_001182061.1:n.*161T=
NM_058195.3:c.*112T= , LRG_11t2:c.*112T=	NP_478102.2:n.*112T=
NM_058197.4:c.742T=	NP_478104.2:n.742T=
XM_005251343.1:c.315T=	XP_005251400.1:p.Asp105=
XM_011517679.1:c.315T=	XP_011515981.1:p.Asp105=
NM_001363763.1:c.315T=	NP_001350692.1:p.Asp105=
NM_001363763.2:c.315T=	NP_001350692.1:p.Asp105=
NM_000077.5:c.468T= MANE Select	NP_000068.1:p.Asp156=
NM_001195132.2:c.*161T=	NP_001182061.1:n.*161T=
NM_058195.4:c.*112T= MANE Plus Clinical	NP_478102.2:n.*112T=
NM_058197.5:c.*391T=	NP_478104.2:n.*391T=