Canonical Allele Identifier: CA1839157888

Gene: CDKN2A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21968182C= , CM000671.2:g.21968182C=	GRCh38
NC_000009.11:g.21968181C= , CM000671.1:g.21968181C=	GRCh37
NC_000009.10:g.21958181C=	NCBI36
NG_007485.1:g.31310G= , LRG_11:g.31310G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304494.10:c.*47G= MANE Select	ENSP00000307101.5:n.*47G=
ENST00000404796.3:c.348-61251C=	ENSP00000385916.2:n.348-61251C=
ENST00000579755.2:c.*162G= MANE Plus Clinical	ENSP00000462950.1:n.*162G=
ENST00000304494.9:c.*47G=	ENSP00000307101.5:n.*47G=
ENST00000361570.4:c.*47G=	ENSP00000355153.4:n.*47G=
ENST00000380151.3:c.792G=	ENSP00000369496.3:n.792G=
ENST00000404796.2:c.348-61251C=	ENSP00000385916.2:n.348-61251C=
ENST00000494262.5:c.*47G=	ENSP00000464952.1:n.*47G=
ENST00000498124.1:c.*211G=	ENSP00000418915.1:n.*211G=
ENST00000498628.6:c.*47G=	ENSP00000467857.1:n.*47G=
ENST00000530628.2:c.*88G=	ENSP00000432664.2:n.*88G=
ENST00000578845.2:c.*47G=	ENSP00000467390.1:n.*47G=
ENST00000579122.1:c.*27G=	ENSP00000464202.1:n.*27G=
ENST00000579755.1:c.*162G=	ENSP00000462950.1:n.*162G=
NM_000077.4:c.*47G= , LRG_11t1:c.*47G=	NP_000068.1:n.*47G=
NM_001195132.1:c.*211G=	NP_001182061.1:n.*211G=
NM_058195.3:c.*162G= , LRG_11t2:c.*162G=	NP_478102.2:n.*162G=
NM_058197.4:c.792G=	NP_478104.2:n.792G=
XM_005251343.1:c.*47G=	XP_005251400.1:n.*47G=
XM_011517679.1:c.*47G=	XP_011515981.1:n.*47G=
NM_001363763.1:c.*47G=	NP_001350692.1:n.*47G=
NM_001363763.2:c.*47G=	NP_001350692.1:n.*47G=
NM_000077.5:c.*47G= MANE Select	NP_000068.1:n.*47G=
NM_001195132.2:c.*211G=	NP_001182061.1:n.*211G=
NM_058195.4:c.*162G= MANE Plus Clinical	NP_478102.2:n.*162G=
NM_058197.5:c.*441G=	NP_478104.2:n.*441G=