Canonical Allele Identifier: CA2689596967

Gene: CDKN2A

Linked Data

• gnomAD v4: 9-21968149-G-GGGGCA

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21968151_21968155dup , CM000671.2:g.21968151_21968155dup	GRCh38
NC_000009.11:g.21968150_21968154dup , CM000671.1:g.21968150_21968154dup	GRCh37
NC_000009.10:g.21958150_21958154dup	NCBI36
NG_007485.1:g.31338_31342dup , LRG_11:g.31338_31342dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304494.10:c.*75_*79dup MANE Select	ENSP00000307101.5:n.*75_*79dup
ENST00000404796.3:c.348-61282_348-61278dup	ENSP00000385916.2:n.348-61282_348-61278dup
ENST00000579755.2:c.*190_*194dup MANE Plus Clinical	ENSP00000462950.1:n.*190_*194dup
ENST00000304494.9:c.*75_*79dup	ENSP00000307101.5:n.*75_*79dup
ENST00000361570.4:c.*75_*79dup	ENSP00000355153.4:n.*75_*79dup
ENST00000404796.2:c.348-61282_348-61278dup	ENSP00000385916.2:n.348-61282_348-61278dup
ENST00000498124.1:c.*239_*243dup	ENSP00000418915.1:n.*239_*243dup
ENST00000498628.6:c.*75_*79dup	ENSP00000467857.1:n.*75_*79dup
ENST00000530628.2:c.*116_*120dup	ENSP00000432664.2:n.*116_*120dup
ENST00000578845.2:c.*75_*79dup	ENSP00000467390.1:n.*75_*79dup
ENST00000579122.1:c.*55_*59dup	ENSP00000464202.1:n.*55_*59dup
ENST00000579755.1:c.*190_*194dup	ENSP00000462950.1:n.*190_*194dup
NM_000077.4:c.*75_*79dup , LRG_11t1:c.*75_*79dup	NP_000068.1:n.*75_*79dup
NM_001195132.1:c.*239_*243dup	NP_001182061.1:n.*239_*243dup
NM_058195.3:c.*190_*194dup , LRG_11t2:c.*190_*194dup	NP_478102.2:n.*190_*194dup
NM_058197.4:c.820_824dup	NP_478104.2:n.820_824dup
XM_005251343.1:c.*75_*79dup	XP_005251400.1:n.*75_*79dup
XM_011517679.1:c.*75_*79dup	XP_011515981.1:n.*75_*79dup
NM_001363763.1:c.*75_*79dup	NP_001350692.1:n.*75_*79dup
NM_001363763.2:c.*75_*79dup	NP_001350692.1:n.*75_*79dup
NM_000077.5:c.*75_*79dup MANE Select	NP_000068.1:n.*75_*79dup
NM_001195132.2:c.*239_*243dup	NP_001182061.1:n.*239_*243dup
NM_058195.4:c.*190_*194dup MANE Plus Clinical	NP_478102.2:n.*190_*194dup
NM_058197.5:c.*469_*473dup	NP_478104.2:n.*469_*473dup