Canonical Allele Identifier: CA2840249438

Gene: CDKN2A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21968164dup , CM000671.2:g.21968164dup	GRCh38
NC_000009.11:g.21968163dup , CM000671.1:g.21968163dup	GRCh37
NC_000009.10:g.21958163dup	NCBI36
NG_007485.1:g.31330dup , LRG_11:g.31330dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304494.10:c.*67dup MANE Select	ENSP00000307101.5:n.*67dup
ENST00000404796.3:c.348-61269dup	ENSP00000385916.2:n.348-61269dup
ENST00000579755.2:c.*182dup MANE Plus Clinical	ENSP00000462950.1:n.*182dup
ENST00000304494.9:c.*67dup	ENSP00000307101.5:n.*67dup
ENST00000361570.4:c.*67dup	ENSP00000355153.4:n.*67dup
ENST00000404796.2:c.348-61269dup	ENSP00000385916.2:n.348-61269dup
ENST00000498124.1:c.*231dup	ENSP00000418915.1:n.*231dup
ENST00000498628.6:c.*67dup	ENSP00000467857.1:n.*67dup
ENST00000530628.2:c.*108dup	ENSP00000432664.2:n.*108dup
ENST00000578845.2:c.*67dup	ENSP00000467390.1:n.*67dup
ENST00000579122.1:c.*47dup	ENSP00000464202.1:n.*47dup
ENST00000579755.1:c.*182dup	ENSP00000462950.1:n.*182dup
NM_000077.4:c.*67dup , LRG_11t1:c.*67dup	NP_000068.1:n.*67dup
NM_001195132.1:c.*231dup	NP_001182061.1:n.*231dup
NM_058195.3:c.*182dup , LRG_11t2:c.*182dup	NP_478102.2:n.*182dup
NM_058197.4:c.812dup	NP_478104.2:n.812dup
XM_005251343.1:c.*67dup	XP_005251400.1:n.*67dup
XM_011517679.1:c.*67dup	XP_011515981.1:n.*67dup
NM_001363763.1:c.*67dup	NP_001350692.1:n.*67dup
NM_001363763.2:c.*67dup	NP_001350692.1:n.*67dup
NM_000077.5:c.*67dup MANE Select	NP_000068.1:n.*67dup
NM_001195132.2:c.*231dup	NP_001182061.1:n.*231dup
NM_058195.4:c.*182dup MANE Plus Clinical	NP_478102.2:n.*182dup
NM_058197.5:c.*461dup	NP_478104.2:n.*461dup