Canonical Allele Identifier: CA2689596957

Gene: CDKN2A

Linked Data

• gnomAD v4: 9-21968146-GC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21968147del , CM000671.2:g.21968147del	GRCh38
NC_000009.11:g.21968146del , CM000671.1:g.21968146del	GRCh37
NC_000009.10:g.21958146del	NCBI36
NG_007485.1:g.31345del , LRG_11:g.31345del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304494.10:c.*82del MANE Select	ENSP00000307101.5:n.*82del
ENST00000404796.3:c.348-61286del	ENSP00000385916.2:n.348-61286del
ENST00000579755.2:c.*197del MANE Plus Clinical	ENSP00000462950.1:n.*197del
ENST00000304494.9:c.*82del	ENSP00000307101.5:n.*82del
ENST00000361570.4:c.*82del	ENSP00000355153.4:n.*82del
ENST00000404796.2:c.348-61286del	ENSP00000385916.2:n.348-61286del
ENST00000498124.1:c.*246del	ENSP00000418915.1:n.*246del
ENST00000498628.6:c.*82del	ENSP00000467857.1:n.*82del
ENST00000530628.2:c.*123del	ENSP00000432664.2:n.*123del
ENST00000578845.2:c.*82del	ENSP00000467390.1:n.*82del
ENST00000579122.1:c.*62del	ENSP00000464202.1:n.*62del
ENST00000579755.1:c.*197del	ENSP00000462950.1:n.*197del
NM_000077.4:c.*82del , LRG_11t1:c.*82del	NP_000068.1:n.*82del
NM_001195132.1:c.*246del	NP_001182061.1:n.*246del
NM_058195.3:c.*197del , LRG_11t2:c.*197del	NP_478102.2:n.*197del
NM_058197.4:c.827del	NP_478104.2:n.827del
XM_005251343.1:c.*82del	XP_005251400.1:n.*82del
XM_011517679.1:c.*82del	XP_011515981.1:n.*82del
NM_001363763.1:c.*82del	NP_001350692.1:n.*82del
NM_001363763.2:c.*82del	NP_001350692.1:n.*82del
NM_000077.5:c.*82del MANE Select	NP_000068.1:n.*82del
NM_001195132.2:c.*246del	NP_001182061.1:n.*246del
NM_058195.4:c.*197del MANE Plus Clinical	NP_478102.2:n.*197del
NM_058197.5:c.*476del	NP_478104.2:n.*476del