Canonical Allele Identifier: CA2689599574

Gene: CDKN2A

Linked Data

• gnomAD v4: 9-21975147-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21975149del , CM000671.2:g.21975149del	GRCh38
NC_000009.11:g.21975148del , CM000671.1:g.21975148del	GRCh37
NC_000009.10:g.21965148del	NCBI36
NG_007485.1:g.24344del , LRG_11:g.24344del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000404796.3:c.348-54284del	ENSP00000385916.2:n.348-54284del
ENST00000579755.2:c.194-3940del MANE Plus Clinical	ENSP00000462950.1:n.194-3940del
ENST00000361570.4:c.194-3940del	ENSP00000355153.4:n.194-3940del
ENST00000404796.2:c.348-54284del	ENSP00000385916.2:n.348-54284del
ENST00000494262.5:c.-3-3940del	ENSP00000464952.1:n.-3-3940del
ENST00000498628.6:c.-3-3940del	ENSP00000467857.1:n.-3-3940del
ENST00000530628.2:c.194-3940del	ENSP00000432664.2:n.194-3940del
ENST00000579755.1:c.194-3940del	ENSP00000462950.1:n.194-3940del
NM_058195.3:c.194-3940del , LRG_11t2:c.194-3940del	NP_478102.2:n.194-3940del
XM_011517675.1:c.-321del	XP_011515977.1:n.-321del
XM_011517676.1:c.-321del	XP_011515978.1:n.-321del
XM_011517679.1:c.-3-3940del	XP_011515981.1:n.-3-3940del
XR_929159.1:n.81del
XR_929161.1:n.341-3940del
XR_929162.1:n.341-3940del
XR_929163.1:n.290-3940del
NM_001363763.1:c.-3-3940del	NP_001350692.1:n.-3-3940del
XM_011517675.2:c.-321del	XP_011515977.1:n.-321del
XM_011517676.2:c.-321del	XP_011515978.1:n.-321del
XR_929159.2:n.10del
NM_001363763.2:c.-3-3940del	NP_001350692.1:n.-3-3940del
NM_058195.4:c.194-3940del MANE Plus Clinical	NP_478102.2:n.194-3940del