Canonical Allele Identifier: CA1839158058

Gene: CDKN2A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21968238G= , CM000671.2:g.21968238G=	GRCh38
NC_000009.11:g.21968237G= , CM000671.1:g.21968237G=	GRCh37
NC_000009.10:g.21958237G=	NCBI36
NG_007485.1:g.31254C= , LRG_11:g.31254C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304494.10:c.462C= MANE Select	ENSP00000307101.5:p.Ile154=
ENST00000404796.3:c.348-61195G=	ENSP00000385916.2:n.348-61195G=
ENST00000579755.2:c.*106C= MANE Plus Clinical	ENSP00000462950.1:n.*106C=
ENST00000304494.9:c.462C=	ENSP00000307101.5:p.Ile154=
ENST00000361570.4:c.504C=	ENSP00000355153.4:p.Ile168=
ENST00000380151.3:c.736C=	ENSP00000369496.3:n.736C=
ENST00000404796.2:c.348-61195G=	ENSP00000385916.2:n.348-61195G=
ENST00000494262.5:c.309C=	ENSP00000464952.1:p.Ile103=
ENST00000498124.1:c.*155C=	ENSP00000418915.1:n.*155C=
ENST00000498628.6:c.309C=	ENSP00000467857.1:p.Ile103=
ENST00000530628.2:c.*32C=	ENSP00000432664.2:n.*32C=
ENST00000578845.2:c.309C=	ENSP00000467390.1:p.Ile103=
ENST00000579122.1:c.388C=	ENSP00000464202.1:p.Pro130=
ENST00000579755.1:c.*106C=	ENSP00000462950.1:n.*106C=
NM_000077.4:c.462C= , LRG_11t1:c.462C=	NP_000068.1:p.Ile154=
NM_001195132.1:c.*155C=	NP_001182061.1:n.*155C=
NM_058195.3:c.*106C= , LRG_11t2:c.*106C=	NP_478102.2:n.*106C=
NM_058197.4:c.736C=	NP_478104.2:n.736C=
XM_005251343.1:c.309C=	XP_005251400.1:p.Ile103=
XM_011517679.1:c.309C=	XP_011515981.1:p.Ile103=
NM_001363763.1:c.309C=	NP_001350692.1:p.Ile103=
NM_001363763.2:c.309C=	NP_001350692.1:p.Ile103=
NM_000077.5:c.462C= MANE Select	NP_000068.1:p.Ile154=
NM_001195132.2:c.*155C=	NP_001182061.1:n.*155C=
NM_058195.4:c.*106C= MANE Plus Clinical	NP_478102.2:n.*106C=
NM_058197.5:c.*385C=	NP_478104.2:n.*385C=