Canonical Allele Identifier: CA2689597042

Gene: CDKN2A

Linked Data

• gnomAD v4: 9-21968194-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21968194G>A , CM000671.2:g.21968194G>A	GRCh38
NC_000009.11:g.21968193G>A , CM000671.1:g.21968193G>A	GRCh37
NC_000009.10:g.21958193G>A	NCBI36
NG_007485.1:g.31298C>T , LRG_11:g.31298C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304494.10:c.*35C>T MANE Select	ENSP00000307101.5:n.*35C>T
ENST00000404796.3:c.348-61239G>A	ENSP00000385916.2:n.348-61239G>A
ENST00000579755.2:c.*150C>T MANE Plus Clinical	ENSP00000462950.1:n.*150C>T
ENST00000304494.9:c.*35C>T	ENSP00000307101.5:n.*35C>T
ENST00000361570.4:c.*35C>T	ENSP00000355153.4:n.*35C>T
ENST00000380151.3:c.780C>T	ENSP00000369496.3:n.780C>T
ENST00000404796.2:c.348-61239G>A	ENSP00000385916.2:n.348-61239G>A
ENST00000494262.5:c.*35C>T	ENSP00000464952.1:n.*35C>T
ENST00000498124.1:c.*199C>T	ENSP00000418915.1:n.*199C>T
ENST00000498628.6:c.*35C>T	ENSP00000467857.1:n.*35C>T
ENST00000530628.2:c.*76C>T	ENSP00000432664.2:n.*76C>T
ENST00000578845.2:c.*35C>T	ENSP00000467390.1:n.*35C>T
ENST00000579122.1:c.*15C>T	ENSP00000464202.1:n.*15C>T
ENST00000579755.1:c.*150C>T	ENSP00000462950.1:n.*150C>T
NM_000077.4:c.*35C>T , LRG_11t1:c.*35C>T	NP_000068.1:n.*35C>T
NM_001195132.1:c.*199C>T	NP_001182061.1:n.*199C>T
NM_058195.3:c.*150C>T , LRG_11t2:c.*150C>T	NP_478102.2:n.*150C>T
NM_058197.4:c.780C>T	NP_478104.2:n.780C>T
XM_005251343.1:c.*35C>T	XP_005251400.1:n.*35C>T
XM_011517679.1:c.*35C>T	XP_011515981.1:n.*35C>T
NM_001363763.1:c.*35C>T	NP_001350692.1:n.*35C>T
NM_001363763.2:c.*35C>T	NP_001350692.1:n.*35C>T
NM_000077.5:c.*35C>T MANE Select	NP_000068.1:n.*35C>T
NM_001195132.2:c.*199C>T	NP_001182061.1:n.*199C>T
NM_058195.4:c.*150C>T MANE Plus Clinical	NP_478102.2:n.*150C>T
NM_058197.5:c.*429C>T	NP_478104.2:n.*429C>T