Canonical Allele Identifier: CA862181935

Gene: CDKN2A

Linked Data

• dbSNP Id: rs1467404677
• gnomAD v3: 9-21986741-GAAGA-G
• gnomAD v4: 9-21986741-GAAGA-G
• MyVariant Identifiers: chr9:g.21986741_21986744del (hg19) ; chr9:g.21986742_21986745del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21986745_21986748del , CM000671.2:g.21986745_21986748del	GRCh38
NC_000009.11:g.21986744_21986747del , CM000671.1:g.21986744_21986747del	GRCh37
NC_000009.10:g.21976744_21976747del	NCBI36
NG_007485.1:g.12747_12750del , LRG_11:g.12747_12750del

Transcript Alleles

HGVS	Amino-acid change
ENST00000404796.3:c.348-42688_348-42685del	ENSP00000385916.2:n.348-42688_348-42685de...
ENST00000579755.2:c.193+7394_193+7397del MANE Plus Clinical	ENSP00000462950.1:n.193+7394_193+7397del
ENST00000361570.4:c.193+7394_193+7397del	ENSP00000355153.4:n.193+7394_193+7397del
ENST00000404796.2:c.348-42688_348-42685del	ENSP00000385916.2:n.348-42688_348-42685de...
ENST00000494262.5:c.-4+7137_-4+7140del	ENSP00000464952.1:n.-4+7137_-4+7140del
ENST00000498628.6:c.-4+8076_-4+8079del	ENSP00000467857.1:n.-4+8076_-4+8079del
ENST00000530628.2:c.193+7394_193+7397del	ENSP00000432664.2:n.193+7394_193+7397del
ENST00000579755.1:c.193+7394_193+7397del	ENSP00000462950.1:n.193+7394_193+7397del
NM_058195.3:c.193+7394_193+7397del , LRG_11t2:c.193+7394_193+7397del	NP_478102.2:n.193+7394_193+7397del
XM_011517679.1:c.-4+8076_-4+8079del	XP_011515981.1:n.-4+8076_-4+8079del
XR_929161.1:n.340+7394_340+7397del
XR_929162.1:n.340+7394_340+7397del
XR_929163.1:n.289+7394_289+7397del
NM_001363763.1:c.-4+8076_-4+8079del	NP_001350692.1:n.-4+8076_-4+8079del
NM_001363763.2:c.-4+8076_-4+8079del	NP_001350692.1:n.-4+8076_-4+8079del
NM_058195.4:c.193+7394_193+7397del MANE Plus Clinical	NP_478102.2:n.193+7394_193+7397del