Canonical Allele Identifier: CA2689599402

Gene: CDKN2A

Linked Data

• gnomAD v4: 9-21974981-T-TG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21974983dup , CM000671.2:g.21974983dup	GRCh38
NC_000009.11:g.21974982dup , CM000671.1:g.21974982dup	GRCh37
NC_000009.10:g.21964982dup	NCBI36
NG_007485.1:g.24510dup , LRG_11:g.24510dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000404796.3:c.348-54450dup	ENSP00000385916.2:n.348-54450dup
ENST00000579755.2:c.194-3774dup MANE Plus Clinical	ENSP00000462950.1:n.194-3774dup
ENST00000304494.9:c.-155dup	ENSP00000307101.5:n.-155dup
ENST00000361570.4:c.194-3774dup	ENSP00000355153.4:n.194-3774dup
ENST00000404796.2:c.348-54450dup	ENSP00000385916.2:n.348-54450dup
ENST00000494262.5:c.-3-3774dup	ENSP00000464952.1:n.-3-3774dup
ENST00000498628.6:c.-3-3774dup	ENSP00000467857.1:n.-3-3774dup
ENST00000530628.2:c.194-3774dup	ENSP00000432664.2:n.194-3774dup
ENST00000579755.1:c.194-3774dup	ENSP00000462950.1:n.194-3774dup
NM_000077.4:c.-155dup , LRG_11t1:c.-155dup	NP_000068.1:n.-155dup
NM_001195132.1:c.-155dup	NP_001182061.1:n.-155dup
NM_058195.3:c.194-3774dup , LRG_11t2:c.194-3774dup	NP_478102.2:n.194-3774dup
XM_011517675.1:c.-155dup	XP_011515977.1:n.-155dup
XM_011517676.1:c.-155dup	XP_011515978.1:n.-155dup
XM_011517679.1:c.-3-3774dup	XP_011515981.1:n.-3-3774dup
XR_929159.1:n.247dup
XR_929161.1:n.341-3774dup
XR_929162.1:n.341-3774dup
XR_929163.1:n.290-3774dup
NM_001363763.1:c.-3-3774dup	NP_001350692.1:n.-3-3774dup
XM_011517675.2:c.-155dup	XP_011515977.1:n.-155dup
XM_011517676.2:c.-155dup	XP_011515978.1:n.-155dup
XR_929159.2:n.176dup
NM_001363763.2:c.-3-3774dup	NP_001350692.1:n.-3-3774dup
NM_058195.4:c.194-3774dup MANE Plus Clinical	NP_478102.2:n.194-3774dup