Canonical Allele Identifier: CA1839158002

Gene: CDKN2A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21968223G= , CM000671.2:g.21968223G=	GRCh38
NC_000009.11:g.21968222G= , CM000671.1:g.21968222G=	GRCh37
NC_000009.10:g.21958222G=	NCBI36
NG_007485.1:g.31269C= , LRG_11:g.31269C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304494.10:c.*6C= MANE Select	ENSP00000307101.5:n.*6C=
ENST00000404796.3:c.348-61210G=	ENSP00000385916.2:n.348-61210G=
ENST00000579755.2:c.*121C= MANE Plus Clinical	ENSP00000462950.1:n.*121C=
ENST00000304494.9:c.*6C=	ENSP00000307101.5:n.*6C=
ENST00000361570.4:c.*6C=	ENSP00000355153.4:n.*6C=
ENST00000380151.3:c.751C=	ENSP00000369496.3:n.751C=
ENST00000404796.2:c.348-61210G=	ENSP00000385916.2:n.348-61210G=
ENST00000494262.5:c.*6C=	ENSP00000464952.1:n.*6C=
ENST00000498124.1:c.*170C=	ENSP00000418915.1:n.*170C=
ENST00000498628.6:c.*6C=	ENSP00000467857.1:n.*6C=
ENST00000530628.2:c.*47C=	ENSP00000432664.2:n.*47C=
ENST00000578845.2:c.*6C=	ENSP00000467390.1:n.*6C=
ENST00000579122.1:c.403C=	ENSP00000464202.1:p.Pro135=
ENST00000579755.1:c.*121C=	ENSP00000462950.1:n.*121C=
NM_000077.4:c.*6C= , LRG_11t1:c.*6C=	NP_000068.1:n.*6C=
NM_001195132.1:c.*170C=	NP_001182061.1:n.*170C=
NM_058195.3:c.*121C= , LRG_11t2:c.*121C=	NP_478102.2:n.*121C=
NM_058197.4:c.751C=	NP_478104.2:n.751C=
XM_005251343.1:c.*6C=	XP_005251400.1:n.*6C=
XM_011517679.1:c.*6C=	XP_011515981.1:n.*6C=
NM_001363763.1:c.*6C=	NP_001350692.1:n.*6C=
NM_001363763.2:c.*6C=	NP_001350692.1:n.*6C=
NM_000077.5:c.*6C= MANE Select	NP_000068.1:n.*6C=
NM_001195132.2:c.*170C=	NP_001182061.1:n.*170C=
NM_058195.4:c.*121C= MANE Plus Clinical	NP_478102.2:n.*121C=
NM_058197.5:c.*400C=	NP_478104.2:n.*400C=