Canonical Allele Identifier: CA190727772

Gene: CDKN2A

Linked Data

• dbSNP Id: rs770191005
• gnomAD v2: 9-21967988-GGT-G
• gnomAD v3: 9-21967989-GGT-G
• gnomAD v4: 9-21967989-GGT-G
• MyVariant Identifiers: chr9:g.21967989_21967990del (hg19) ; chr9:g.21967990_21967991del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21967992_21967993del , CM000671.2:g.21967992_21967993del	GRCh38
NC_000009.11:g.21967991_21967992del , CM000671.1:g.21967991_21967992del	GRCh37
NC_000009.10:g.21957991_21957992del	NCBI36
NG_007485.1:g.31501_31502del , LRG_11:g.31501_31502del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304494.10:c.*238_*239del MANE Select	ENSP00000307101.5:n.*238_*239del
ENST00000404796.3:c.348-61441_348-61440del	ENSP00000385916.2:n.348-61441_348-61440del
ENST00000579755.2:c.*353_*354del MANE Plus Clinical	ENSP00000462950.1:n.*353_*354del
ENST00000304494.9:c.*238_*239del	ENSP00000307101.5:n.*238_*239del
ENST00000361570.4:c.*238_*239del	ENSP00000355153.4:n.*238_*239del
ENST00000404796.2:c.348-61441_348-61440del	ENSP00000385916.2:n.348-61441_348-61440del
ENST00000579755.1:c.*353_*354del	ENSP00000462950.1:n.*353_*354del
NM_000077.4:c.*238_*239del , LRG_11t1:c.*238_*239del	NP_000068.1:n.*238_*239del
NM_001195132.1:c.*402_*403del	NP_001182061.1:n.*402_*403del
NM_058195.3:c.*353_*354del , LRG_11t2:c.*353_*354del	NP_478102.2:n.*353_*354del
NM_058197.4:c.983_984del	NP_478104.2:n.983_984del
XM_005251343.1:c.*238_*239del	XP_005251400.1:n.*238_*239del
XM_011517679.1:c.*238_*239del	XP_011515981.1:n.*238_*239del
NM_001363763.1:c.*238_*239del	NP_001350692.1:n.*238_*239del
NM_001363763.2:c.*238_*239del	NP_001350692.1:n.*238_*239del
NM_000077.5:c.*238_*239del MANE Select	NP_000068.1:n.*238_*239del
NM_001195132.2:c.*402_*403del	NP_001182061.1:n.*402_*403del
NM_058195.4:c.*353_*354del MANE Plus Clinical	NP_478102.2:n.*353_*354del
NM_058197.5:c.*632_*633del	NP_478104.2:n.*632_*633del