Canonical Allele Identifier: CA2689596987

Gene: CDKN2A

Linked Data

• gnomAD v4: 9-21968159-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21968161del , CM000671.2:g.21968161del	GRCh38
NC_000009.11:g.21968160del , CM000671.1:g.21968160del	GRCh37
NC_000009.10:g.21958160del	NCBI36
NG_007485.1:g.31332del , LRG_11:g.31332del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304494.10:c.*69del MANE Select	ENSP00000307101.5:n.*69del
ENST00000404796.3:c.348-61272del	ENSP00000385916.2:n.348-61272del
ENST00000579755.2:c.*184del MANE Plus Clinical	ENSP00000462950.1:n.*184del
ENST00000304494.9:c.*69del	ENSP00000307101.5:n.*69del
ENST00000361570.4:c.*69del	ENSP00000355153.4:n.*69del
ENST00000404796.2:c.348-61272del	ENSP00000385916.2:n.348-61272del
ENST00000498124.1:c.*233del	ENSP00000418915.1:n.*233del
ENST00000498628.6:c.*69del	ENSP00000467857.1:n.*69del
ENST00000530628.2:c.*110del	ENSP00000432664.2:n.*110del
ENST00000578845.2:c.*69del	ENSP00000467390.1:n.*69del
ENST00000579122.1:c.*49del	ENSP00000464202.1:n.*49del
ENST00000579755.1:c.*184del	ENSP00000462950.1:n.*184del
NM_000077.4:c.*69del , LRG_11t1:c.*69del	NP_000068.1:n.*69del
NM_001195132.1:c.*233del	NP_001182061.1:n.*233del
NM_058195.3:c.*184del , LRG_11t2:c.*184del	NP_478102.2:n.*184del
NM_058197.4:c.814del	NP_478104.2:n.814del
XM_005251343.1:c.*69del	XP_005251400.1:n.*69del
XM_011517679.1:c.*69del	XP_011515981.1:n.*69del
NM_001363763.1:c.*69del	NP_001350692.1:n.*69del
NM_001363763.2:c.*69del	NP_001350692.1:n.*69del
NM_000077.5:c.*69del MANE Select	NP_000068.1:n.*69del
NM_001195132.2:c.*233del	NP_001182061.1:n.*233del
NM_058195.4:c.*184del MANE Plus Clinical	NP_478102.2:n.*184del
NM_058197.5:c.*463del	NP_478104.2:n.*463del