Canonical Allele Identifier: CA652685568

Gene: CDKN2A

Linked Data

• dbSNP Id: rs2131079188
• gnomAD v4: 9-21968200-C-CG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21968201dup , CM000671.2:g.21968201dup	GRCh38
NC_000009.11:g.21968200dup , CM000671.1:g.21968200dup	GRCh37
NC_000009.10:g.21958200dup	NCBI36
NG_007485.1:g.31291dup , LRG_11:g.31291dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304494.10:c.*28dup MANE Select	ENSP00000307101.5:n.*28dup
ENST00000404796.3:c.348-61232dup	ENSP00000385916.2:n.348-61232dup
ENST00000579755.2:c.*143dup MANE Plus Clinical	ENSP00000462950.1:n.*143dup
ENST00000304494.9:c.*28dup	ENSP00000307101.5:n.*28dup
ENST00000361570.4:c.*28dup	ENSP00000355153.4:n.*28dup
ENST00000380151.3:c.773dup	ENSP00000369496.3:n.773dup
ENST00000404796.2:c.348-61232dup	ENSP00000385916.2:n.348-61232dup
ENST00000494262.5:c.*28dup	ENSP00000464952.1:n.*28dup
ENST00000498124.1:c.*192dup	ENSP00000418915.1:n.*192dup
ENST00000498628.6:c.*28dup	ENSP00000467857.1:n.*28dup
ENST00000530628.2:c.*69dup	ENSP00000432664.2:n.*69dup
ENST00000578845.2:c.*28dup	ENSP00000467390.1:n.*28dup
ENST00000579122.1:c.*8dup	ENSP00000464202.1:n.*8dup
ENST00000579755.1:c.*143dup	ENSP00000462950.1:n.*143dup
NM_000077.4:c.*28dup , LRG_11t1:c.*28dup	NP_000068.1:n.*28dup
NM_001195132.1:c.*192dup	NP_001182061.1:n.*192dup
NM_058195.3:c.*143dup , LRG_11t2:c.*143dup	NP_478102.2:n.*143dup
NM_058197.4:c.773dup	NP_478104.2:n.773dup
XM_005251343.1:c.*28dup	XP_005251400.1:n.*28dup
XM_011517679.1:c.*28dup	XP_011515981.1:n.*28dup
NM_001363763.1:c.*28dup	NP_001350692.1:n.*28dup
NM_001363763.2:c.*28dup	NP_001350692.1:n.*28dup
NM_000077.5:c.*28dup MANE Select	NP_000068.1:n.*28dup
NM_001195132.2:c.*192dup	NP_001182061.1:n.*192dup
NM_058195.4:c.*143dup MANE Plus Clinical	NP_478102.2:n.*143dup
NM_058197.5:c.*422dup	NP_478104.2:n.*422dup