Canonical Allele Identifier: CA645552625

Gene: CDKN2A

Linked Data

• COSMIC: COSM13461

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21974770_21974775del , CM000671.2:g.21974770_21974775del	GRCh38
NC_000009.11:g.21974769_21974774del , CM000671.1:g.21974769_21974774del	GRCh37
NC_000009.10:g.21964769_21964774del	NCBI36
NG_007485.1:g.24722_24727del , LRG_11:g.24722_24727del

Transcript Alleles

HGVS	Amino-acid change
ENST00000304494.10:c.58_63del MANE Select	ENSP00000307101.5:p.Ala20_Ala21del
ENST00000404796.3:c.348-54663_348-54658del	ENSP00000385916.2:n.348-54663_348-54658de...
ENST00000579755.2:c.194-3562_194-3557del MANE Plus Clinical	ENSP00000462950.1:n.194-3562_194-3557del
ENST00000304494.9:c.58_63del	ENSP00000307101.5:p.Ala20_Ala21del
ENST00000361570.4:c.194-3562_194-3557del	ENSP00000355153.4:n.194-3562_194-3557del
ENST00000380151.3:c.58_63del	ENSP00000369496.3:p.Ala20_Ala21del
ENST00000404796.2:c.348-54663_348-54658del	ENSP00000385916.2:n.348-54663_348-54658de...
ENST00000494262.5:c.-3-3562_-3-3557del	ENSP00000464952.1:n.-3-3562_-3-3557del
ENST00000498124.1:c.58_63del	ENSP00000418915.1:p.Ala20_Ala21del
ENST00000498628.6:c.-3-3562_-3-3557del	ENSP00000467857.1:n.-3-3562_-3-3557del
ENST00000530628.2:c.194-3562_194-3557del	ENSP00000432664.2:n.194-3562_194-3557del
ENST00000579122.1:c.58_63del	ENSP00000464202.1:p.Ala20_Ala21del
ENST00000579755.1:c.194-3562_194-3557del	ENSP00000462950.1:n.194-3562_194-3557del
NM_000077.4:c.58_63del , LRG_11t1:c.58_63del	NP_000068.1:p.Ala20_Ala21del
NM_001195132.1:c.58_63del	NP_001182061.1:p.Ala20_Ala21del
NM_058195.3:c.194-3562_194-3557del , LRG_11t2:c.194-3562_194-3557del	NP_478102.2:n.194-3562_194-3557del
NM_058197.4:c.58_63del	NP_478104.2:p.Ala20_Ala21del
XM_011517675.1:c.58_63del	XP_011515977.1:p.Ala20_Ala21del
XM_011517676.1:c.58_63del	XP_011515978.1:p.Ala20_Ala21del
XM_011517679.1:c.-3-3562_-3-3557del	XP_011515981.1:n.-3-3562_-3-3557del
XR_929159.1:n.459_464del
XR_929161.1:n.341-3562_341-3557del
XR_929162.1:n.341-3562_341-3557del
XR_929163.1:n.290-3562_290-3557del
NM_001363763.1:c.-3-3562_-3-3557del	NP_001350692.1:n.-3-3562_-3-3557del
XM_011517675.2:c.58_63del	XP_011515977.1:p.Ala20_Ala21del
XM_011517676.2:c.58_63del	XP_011515978.1:p.Ala20_Ala21del
XR_929159.2:n.388_393del
NM_001363763.2:c.-3-3562_-3-3557del	NP_001350692.1:n.-3-3562_-3-3557del
NM_000077.5:c.58_63del MANE Select	NP_000068.1:p.Ala20_Ala21del
NM_001195132.2:c.58_63del	NP_001182061.1:p.Ala20_Ala21del
NM_058195.4:c.194-3562_194-3557del MANE Plus Clinical	NP_478102.2:n.194-3562_194-3557del
NM_058197.5:c.58_63del	NP_478104.2:p.Ala20_Ala21del