Canonical Allele Identifier: CA2689599259

Gene: CDKN2A

Linked Data

• dbSNP Id: rs2131114652
• gnomAD v4: 9-21974856-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21974861del , CM000671.2:g.21974861del	GRCh38
NC_000009.11:g.21974860del , CM000671.1:g.21974860del	GRCh37
NC_000009.10:g.21964860del	NCBI36
NG_007485.1:g.24635del , LRG_11:g.24635del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000404796.3:c.348-54572del	ENSP00000385916.2:n.348-54572del
ENST00000579755.2:c.194-3649del MANE Plus Clinical	ENSP00000462950.1:n.194-3649del
ENST00000304494.9:c.-30del	ENSP00000307101.5:n.-30del
ENST00000361570.4:c.194-3649del	ENSP00000355153.4:n.194-3649del
ENST00000404796.2:c.348-54572del	ENSP00000385916.2:n.348-54572del
ENST00000494262.5:c.-3-3649del	ENSP00000464952.1:n.-3-3649del
ENST00000498124.1:c.-30del	ENSP00000418915.1:n.-30del
ENST00000498628.6:c.-3-3649del	ENSP00000467857.1:n.-3-3649del
ENST00000530628.2:c.194-3649del	ENSP00000432664.2:n.194-3649del
ENST00000579755.1:c.194-3649del	ENSP00000462950.1:n.194-3649del
NM_000077.4:c.-30del , LRG_11t1:c.-30del	NP_000068.1:n.-30del
NM_001195132.1:c.-30del	NP_001182061.1:n.-30del
NM_058195.3:c.194-3649del , LRG_11t2:c.194-3649del	NP_478102.2:n.194-3649del
XM_011517675.1:c.-30del	XP_011515977.1:n.-30del
XM_011517676.1:c.-30del	XP_011515978.1:n.-30del
XM_011517679.1:c.-3-3649del	XP_011515981.1:n.-3-3649del
XR_929159.1:n.372del
XR_929161.1:n.341-3649del
XR_929162.1:n.341-3649del
XR_929163.1:n.290-3649del
NM_001363763.1:c.-3-3649del	NP_001350692.1:n.-3-3649del
XM_011517675.2:c.-30del	XP_011515977.1:n.-30del
XM_011517676.2:c.-30del	XP_011515978.1:n.-30del
XR_929159.2:n.301del
NM_001363763.2:c.-3-3649del	NP_001350692.1:n.-3-3649del
NM_058195.4:c.194-3649del MANE Plus Clinical	NP_478102.2:n.194-3649del