Canonical Allele Identifier: CA2528430943

Gene: CDKN2A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21968069del , CM000671.2:g.21968069del	GRCh38
NC_000009.11:g.21968068del , CM000671.1:g.21968068del	GRCh37
NC_000009.10:g.21958068del	NCBI36
NG_007485.1:g.31423del , LRG_11:g.31423del

Transcript Alleles

HGVS	Amino-acid change
ENST00000304494.10:c.*160del MANE Select	ENSP00000307101.5:n.*160del
ENST00000404796.3:c.348-61364del	ENSP00000385916.2:n.348-61364del
ENST00000579755.2:c.*275del MANE Plus Clinical	ENSP00000462950.1:n.*275del
ENST00000304494.9:c.*160del	ENSP00000307101.5:n.*160del
ENST00000361570.4:c.*160del	ENSP00000355153.4:n.*160del
ENST00000404796.2:c.348-61364del	ENSP00000385916.2:n.348-61364del
ENST00000498124.1:c.*324del	ENSP00000418915.1:n.*324del
ENST00000530628.2:c.*201del	ENSP00000432664.2:n.*201del
ENST00000578845.2:c.*160del	ENSP00000467390.1:n.*160del
ENST00000579122.1:c.*140del	ENSP00000464202.1:n.*140del
ENST00000579755.1:c.*275del	ENSP00000462950.1:n.*275del
NM_000077.4:c.*160del , LRG_11t1:c.*160del	NP_000068.1:n.*160del
NM_001195132.1:c.*324del	NP_001182061.1:n.*324del
NM_058195.3:c.*275del , LRG_11t2:c.*275del	NP_478102.2:n.*275del
NM_058197.4:c.905del	NP_478104.2:n.905del
XM_005251343.1:c.*160del	XP_005251400.1:n.*160del
XM_011517679.1:c.*160del	XP_011515981.1:n.*160del
NM_001363763.1:c.*160del	NP_001350692.1:n.*160del
NM_001363763.2:c.*160del	NP_001350692.1:n.*160del
NM_000077.5:c.*160del MANE Select	NP_000068.1:n.*160del
NM_001195132.2:c.*324del	NP_001182061.1:n.*324del
NM_058195.4:c.*275del MANE Plus Clinical	NP_478102.2:n.*275del
NM_058197.5:c.*554del	NP_478104.2:n.*554del