Canonical Allele Identifier: CA645552469

Gene: CDKN2A

Linked Data

• COSMIC: COSM13437

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21971090_21971110del , CM000671.2:g.21971090_21971110del	GRCh38
NC_000009.11:g.21971089_21971109del , CM000671.1:g.21971089_21971109del	GRCh37
NC_000009.10:g.21961089_21961109del	NCBI36
NG_007485.1:g.28383_28403del , LRG_11:g.28383_28403del

Transcript Alleles

HGVS	Amino-acid change
ENST00000304494.10:c.250_270del MANE Select	ENSP00000307101.5:p.Asp84_Phe90del
ENST00000404796.3:c.348-58343_348-58323del	ENSP00000385916.2:n.348-58343_348-58323de...
ENST00000579755.2:c.293_313del MANE Plus Clinical	ENSP00000462950.1:p.Arg98_Leu104del
ENST00000304494.9:c.250_270del	ENSP00000307101.5:p.Asp84_Phe90del
ENST00000361570.4:c.292_312del	ENSP00000355153.4:p.Asp98_Phe104del
ENST00000380150.2:n.224_244del
ENST00000380151.3:c.524_544del	ENSP00000369496.3:n.524_544del
ENST00000404796.2:c.348-58343_348-58323del	ENSP00000385916.2:n.348-58343_348-58323de...
ENST00000479692.2:c.97_117del	ENSP00000466887.1:p.Asp33_Phe39del
ENST00000494262.5:c.97_117del	ENSP00000464952.1:p.Asp33_Phe39del
ENST00000497750.1:c.97_117del	ENSP00000468510.1:p.Asp33_Phe39del
ENST00000498124.1:c.250_270del	ENSP00000418915.1:p.Asp84_Phe90del
ENST00000498628.6:c.97_117del	ENSP00000467857.1:p.Asp33_Phe39del
ENST00000530628.2:c.293_313del	ENSP00000432664.2:p.Arg98_Leu104del
ENST00000578845.2:c.97_117del	ENSP00000467390.1:p.Asp33_Phe39del
ENST00000579122.1:c.250_270del	ENSP00000464202.1:p.Asp84_Phe90del
ENST00000579755.1:c.293_313del	ENSP00000462950.1:p.Arg98_Leu104del
NM_000077.4:c.250_270del , LRG_11t1:c.250_270del	NP_000068.1:p.Asp84_Phe90del
NM_001195132.1:c.250_270del	NP_001182061.1:p.Asp84_Phe90del
NM_058195.3:c.293_313del , LRG_11t2:c.293_313del	NP_478102.2:p.Arg98_Leu104del
NM_058197.4:c.524_544del	NP_478104.2:n.524_544del
XM_005251343.1:c.97_117del	XP_005251400.1:p.Asp33_Phe39del
XM_011517675.1:c.250_270del	XP_011515977.1:p.Asp84_Phe90del
XM_011517676.1:c.250_270del	XP_011515978.1:p.Asp84_Phe90del
XM_011517679.1:c.97_117del	XP_011515981.1:p.Asp33_Phe39del
XR_929159.1:n.651_671del
XR_929161.1:n.440_460del
XR_929162.1:n.440_460del
XR_929163.1:n.389_409del
XR_929164.1:n.172_192del
NM_001363763.1:c.97_117del	NP_001350692.1:p.Asp33_Phe39del
XM_011517675.2:c.250_270del	XP_011515977.1:p.Asp84_Phe90del
XM_011517676.2:c.250_270del	XP_011515978.1:p.Asp84_Phe90del
XR_929159.2:n.580_600del
NM_001363763.2:c.97_117del	NP_001350692.1:p.Asp33_Phe39del
NM_000077.5:c.250_270del MANE Select	NP_000068.1:p.Asp84_Phe90del
NM_001195132.2:c.250_270del	NP_001182061.1:p.Asp84_Phe90del
NM_058195.4:c.293_313del MANE Plus Clinical	NP_478102.2:p.Arg98_Leu104del
NM_058197.5:c.*173_*193del	NP_478104.2:n.*173_*193del