Canonical Allele Identifier: CA1122183962

Gene: CDKN2A

Linked Data

• dbSNP Id: rs1819502592
• gnomAD v3: 9-21968204-GT-G
• gnomAD v4: 9-21968204-GT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21968207del , CM000671.2:g.21968207del	GRCh38
NC_000009.11:g.21968206del , CM000671.1:g.21968206del	GRCh37
NC_000009.10:g.21958206del	NCBI36
NG_007485.1:g.31287del , LRG_11:g.31287del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304494.10:c.*24del MANE Select	ENSP00000307101.5:n.*24del
ENST00000404796.3:c.348-61226del	ENSP00000385916.2:n.348-61226del
ENST00000579755.2:c.*139del MANE Plus Clinical	ENSP00000462950.1:n.*139del
ENST00000304494.9:c.*24del	ENSP00000307101.5:n.*24del
ENST00000361570.4:c.*24del	ENSP00000355153.4:n.*24del
ENST00000380151.3:c.769del	ENSP00000369496.3:n.769del
ENST00000404796.2:c.348-61226del	ENSP00000385916.2:n.348-61226del
ENST00000494262.5:c.*24del	ENSP00000464952.1:n.*24del
ENST00000498124.1:c.*188del	ENSP00000418915.1:n.*188del
ENST00000498628.6:c.*24del	ENSP00000467857.1:n.*24del
ENST00000530628.2:c.*65del	ENSP00000432664.2:n.*65del
ENST00000578845.2:c.*24del	ENSP00000467390.1:n.*24del
ENST00000579122.1:c.*4del	ENSP00000464202.1:n.*4del
ENST00000579755.1:c.*139del	ENSP00000462950.1:n.*139del
NM_000077.4:c.*24del , LRG_11t1:c.*24del	NP_000068.1:n.*24del
NM_001195132.1:c.*188del	NP_001182061.1:n.*188del
NM_058195.3:c.*139del , LRG_11t2:c.*139del	NP_478102.2:n.*139del
NM_058197.4:c.769del	NP_478104.2:n.769del
XM_005251343.1:c.*24del	XP_005251400.1:n.*24del
XM_011517679.1:c.*24del	XP_011515981.1:n.*24del
NM_001363763.1:c.*24del	NP_001350692.1:n.*24del
NM_001363763.2:c.*24del	NP_001350692.1:n.*24del
NM_000077.5:c.*24del MANE Select	NP_000068.1:n.*24del
NM_001195132.2:c.*188del	NP_001182061.1:n.*188del
NM_058195.4:c.*139del MANE Plus Clinical	NP_478102.2:n.*139del
NM_058197.5:c.*418del	NP_478104.2:n.*418del