Canonical Allele Identifier: CA2689596813

Gene: CDKN2A

Linked Data

• gnomAD v4: 9-21967992-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21967992G>A , CM000671.2:g.21967992G>A	GRCh38
NC_000009.11:g.21967991G>A , CM000671.1:g.21967991G>A	GRCh37
NC_000009.10:g.21957991G>A	NCBI36
NG_007485.1:g.31500C>T , LRG_11:g.31500C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304494.10:c.*237C>T MANE Select	ENSP00000307101.5:n.*237C>T
ENST00000404796.3:c.348-61441G>A	ENSP00000385916.2:n.348-61441G>A
ENST00000579755.2:c.*352C>T MANE Plus Clinical	ENSP00000462950.1:n.*352C>T
ENST00000304494.9:c.*237C>T	ENSP00000307101.5:n.*237C>T
ENST00000361570.4:c.*237C>T	ENSP00000355153.4:n.*237C>T
ENST00000404796.2:c.348-61441G>A	ENSP00000385916.2:n.348-61441G>A
ENST00000579122.1:c.*217C>T	ENSP00000464202.1:n.*217C>T
ENST00000579755.1:c.*352C>T	ENSP00000462950.1:n.*352C>T
NM_000077.4:c.*237C>T , LRG_11t1:c.*237C>T	NP_000068.1:n.*237C>T
NM_001195132.1:c.*401C>T	NP_001182061.1:n.*401C>T
NM_058195.3:c.*352C>T , LRG_11t2:c.*352C>T	NP_478102.2:n.*352C>T
NM_058197.4:c.982C>T	NP_478104.2:n.982C>T
XM_005251343.1:c.*237C>T	XP_005251400.1:n.*237C>T
XM_011517679.1:c.*237C>T	XP_011515981.1:n.*237C>T
NM_001363763.1:c.*237C>T	NP_001350692.1:n.*237C>T
NM_001363763.2:c.*237C>T	NP_001350692.1:n.*237C>T
NM_000077.5:c.*237C>T MANE Select	NP_000068.1:n.*237C>T
NM_001195132.2:c.*401C>T	NP_001182061.1:n.*401C>T
NM_058195.4:c.*352C>T MANE Plus Clinical	NP_478102.2:n.*352C>T
NM_058197.5:c.*631C>T	NP_478104.2:n.*631C>T