Canonical Allele Identifier: CA862183479

Gene: CDKN2A

Linked Data

• dbSNP Id: rs1168090854
• gnomAD v3: 9-21988804-TG-T
• gnomAD v4: 9-21988804-TG-T
• MyVariant Identifiers: chr9:g.21988804del (hg19) ; chr9:g.21988805del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21988805del , CM000671.2:g.21988805del	GRCh38
NC_000009.11:g.21988804del , CM000671.1:g.21988804del	GRCh37
NC_000009.10:g.21978804del	NCBI36
NG_007485.1:g.10687del , LRG_11:g.10687del

Transcript Alleles

HGVS	Amino-acid change
ENST00000404796.3:c.348-40628del	ENSP00000385916.2:n.348-40628del
ENST00000579755.2:c.193+5334del MANE Plus Clinical	ENSP00000462950.1:n.193+5334del
ENST00000361570.4:c.193+5334del	ENSP00000355153.4:n.193+5334del
ENST00000404796.2:c.348-40628del	ENSP00000385916.2:n.348-40628del
ENST00000494262.5:c.-4+5077del	ENSP00000464952.1:n.-4+5077del
ENST00000498628.6:c.-4+6016del	ENSP00000467857.1:n.-4+6016del
ENST00000530628.2:c.193+5334del	ENSP00000432664.2:n.193+5334del
ENST00000579755.1:c.193+5334del	ENSP00000462950.1:n.193+5334del
NM_058195.3:c.193+5334del , LRG_11t2:c.193+5334del	NP_478102.2:n.193+5334del
XM_011517678.1:c.*1125del	XP_011515980.1:n.*1125del
XM_011517679.1:c.-4+6016del	XP_011515981.1:n.-4+6016del
XR_929161.1:n.340+5334del
XR_929162.1:n.340+5334del
XR_929163.1:n.289+5334del
NM_001363763.1:c.-4+6016del	NP_001350692.1:n.-4+6016del
NM_001363763.2:c.-4+6016del	NP_001350692.1:n.-4+6016del
NM_058195.4:c.193+5334del MANE Plus Clinical	NP_478102.2:n.193+5334del