Canonical Allele Identifier: CA2689599604

Gene: CDKN2A

Linked Data

• gnomAD v4: 9-21975170-CCT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21975172_21975173del , CM000671.2:g.21975172_21975173del	GRCh38
NC_000009.11:g.21975171_21975172del , CM000671.1:g.21975171_21975172del	GRCh37
NC_000009.10:g.21965171_21965172del	NCBI36
NG_007485.1:g.24320_24321del , LRG_11:g.24320_24321del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000404796.3:c.348-54261_348-54260del	ENSP00000385916.2:n.348-54261_348-54260del
ENST00000579755.2:c.194-3964_194-3963del MANE Plus Clinical	ENSP00000462950.1:n.194-3964_194-3963del
ENST00000361570.4:c.194-3964_194-3963del	ENSP00000355153.4:n.194-3964_194-3963del
ENST00000404796.2:c.348-54261_348-54260del	ENSP00000385916.2:n.348-54261_348-54260del
ENST00000494262.5:c.-3-3964_-3-3963del	ENSP00000464952.1:n.-3-3964_-3-3963del
ENST00000498628.6:c.-3-3964_-3-3963del	ENSP00000467857.1:n.-3-3964_-3-3963del
ENST00000530628.2:c.194-3964_194-3963del	ENSP00000432664.2:n.194-3964_194-3963del
ENST00000579755.1:c.194-3964_194-3963del	ENSP00000462950.1:n.194-3964_194-3963del
NM_058195.3:c.194-3964_194-3963del , LRG_11t2:c.194-3964_194-3963del	NP_478102.2:n.194-3964_194-3963del
XM_011517675.1:c.-345_-344del	XP_011515977.1:n.-345_-344del
XM_011517676.1:c.-345_-344del	XP_011515978.1:n.-345_-344del
XM_011517679.1:c.-3-3964_-3-3963del	XP_011515981.1:n.-3-3964_-3-3963del
XR_929159.1:n.57_58del
XR_929161.1:n.341-3964_341-3963del
XR_929162.1:n.341-3964_341-3963del
XR_929163.1:n.290-3964_290-3963del
NM_001363763.1:c.-3-3964_-3-3963del	NP_001350692.1:n.-3-3964_-3-3963del
NM_001363763.2:c.-3-3964_-3-3963del	NP_001350692.1:n.-3-3964_-3-3963del
NM_058195.4:c.194-3964_194-3963del MANE Plus Clinical	NP_478102.2:n.194-3964_194-3963del