Canonical Allele Identifier: CA2689596914

Gene: CDKN2A

Linked Data

• gnomAD v4: 9-21968092-AT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21968097del , CM000671.2:g.21968097del	GRCh38
NC_000009.11:g.21968096del , CM000671.1:g.21968096del	GRCh37
NC_000009.10:g.21958096del	NCBI36
NG_007485.1:g.31399del , LRG_11:g.31399del

Transcript Alleles

HGVS	Amino-acid change
ENST00000304494.10:c.*136del MANE Select	ENSP00000307101.5:n.*136del
ENST00000404796.3:c.348-61336del	ENSP00000385916.2:n.348-61336del
ENST00000579755.2:c.*251del MANE Plus Clinical	ENSP00000462950.1:n.*251del
ENST00000304494.9:c.*136del	ENSP00000307101.5:n.*136del
ENST00000361570.4:c.*136del	ENSP00000355153.4:n.*136del
ENST00000404796.2:c.348-61336del	ENSP00000385916.2:n.348-61336del
ENST00000498124.1:c.*300del	ENSP00000418915.1:n.*300del
ENST00000530628.2:c.*177del	ENSP00000432664.2:n.*177del
ENST00000578845.2:c.*136del	ENSP00000467390.1:n.*136del
ENST00000579122.1:c.*116del	ENSP00000464202.1:n.*116del
ENST00000579755.1:c.*251del	ENSP00000462950.1:n.*251del
NM_000077.4:c.*136del , LRG_11t1:c.*136del	NP_000068.1:n.*136del
NM_001195132.1:c.*300del	NP_001182061.1:n.*300del
NM_058195.3:c.*251del , LRG_11t2:c.*251del	NP_478102.2:n.*251del
NM_058197.4:c.881del	NP_478104.2:n.881del
XM_005251343.1:c.*136del	XP_005251400.1:n.*136del
XM_011517679.1:c.*136del	XP_011515981.1:n.*136del
NM_001363763.1:c.*136del	NP_001350692.1:n.*136del
NM_001363763.2:c.*136del	NP_001350692.1:n.*136del
NM_000077.5:c.*136del MANE Select	NP_000068.1:n.*136del
NM_001195132.2:c.*300del	NP_001182061.1:n.*300del
NM_058195.4:c.*251del MANE Plus Clinical	NP_478102.2:n.*251del
NM_058197.5:c.*530del	NP_478104.2:n.*530del