Canonical Allele Identifier: CA1839157779

Gene: CDKN2A

Linked Data

• dbSNP Id: rs1819496798
• gnomAD v4: 9-21968113-TA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21968116del , CM000671.2:g.21968116del	GRCh38
NC_000009.11:g.21968115del , CM000671.1:g.21968115del	GRCh37
NC_000009.10:g.21958115del	NCBI36
NG_007485.1:g.31378del , LRG_11:g.31378del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304494.10:c.*115del MANE Select	ENSP00000307101.5:n.*115del
ENST00000404796.3:c.348-61317del	ENSP00000385916.2:n.348-61317del
ENST00000579755.2:c.*230del MANE Plus Clinical	ENSP00000462950.1:n.*230del
ENST00000304494.9:c.*115del	ENSP00000307101.5:n.*115del
ENST00000361570.4:c.*115del	ENSP00000355153.4:n.*115del
ENST00000404796.2:c.348-61317del	ENSP00000385916.2:n.348-61317del
ENST00000498124.1:c.*279del	ENSP00000418915.1:n.*279del
ENST00000498628.6:c.*115del	ENSP00000467857.1:n.*115del
ENST00000530628.2:c.*156del	ENSP00000432664.2:n.*156del
ENST00000578845.2:c.*115del	ENSP00000467390.1:n.*115del
ENST00000579122.1:c.*95del	ENSP00000464202.1:n.*95del
ENST00000579755.1:c.*230del	ENSP00000462950.1:n.*230del
NM_000077.4:c.*115del , LRG_11t1:c.*115del	NP_000068.1:n.*115del
NM_001195132.1:c.*279del	NP_001182061.1:n.*279del
NM_058195.3:c.*230del , LRG_11t2:c.*230del	NP_478102.2:n.*230del
NM_058197.4:c.860del	NP_478104.2:n.860del
XM_005251343.1:c.*115del	XP_005251400.1:n.*115del
XM_011517679.1:c.*115del	XP_011515981.1:n.*115del
NM_001363763.1:c.*115del	NP_001350692.1:n.*115del
NM_001363763.2:c.*115del	NP_001350692.1:n.*115del
NM_000077.5:c.*115del MANE Select	NP_000068.1:n.*115del
NM_001195132.2:c.*279del	NP_001182061.1:n.*279del
NM_058195.4:c.*230del MANE Plus Clinical	NP_478102.2:n.*230del
NM_058197.5:c.*509del	NP_478104.2:n.*509del