Canonical Allele Identifier: CA645552511

Gene: CDKN2A

Linked Data

• COSMIC: COSM13438

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21971135_21971136delinsA , CM000671.2:g.21971135_21971136delinsA	GRCh38
NC_000009.11:g.21971134_21971135delinsA , CM000671.1:g.21971134_21971135delinsA	GRCh37
NC_000009.10:g.21961134_21961135delinsA	NCBI36
NG_007485.1:g.28356_28357delinsT , LRG_11:g.28356_28357delinsT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304494.10:c.223_224delinsT MANE Select	ENSP00000307101.5:p.Pro75SerfsTer?
ENST00000404796.3:c.348-58298_348-58297delinsA	ENSP00000385916.2:n.348-58298_348-58297delinsA
ENST00000579755.2:c.266_267delinsT MANE Plus Clinical	ENSP00000462950.1:p.Pro89LeufsTer?
ENST00000304494.9:c.223_224delinsT	ENSP00000307101.5:p.Pro75SerfsTer?
ENST00000361570.4:c.266_267delinsT	ENSP00000355153.4:p.Pro89LeufsTer?
ENST00000380150.2:n.197_198delinsT
ENST00000380151.3:c.497_498delinsT	ENSP00000369496.3:n.497_498delinsT
ENST00000404796.2:c.348-58298_348-58297delinsA	ENSP00000385916.2:n.348-58298_348-58297delinsA
ENST00000479692.2:c.70_71delinsT	ENSP00000466887.1:p.Pro24SerfsTer?
ENST00000494262.5:c.70_71delinsT	ENSP00000464952.1:p.Pro24SerfsTer?
ENST00000497750.1:c.70_71delinsT	ENSP00000468510.1:p.Pro24SerfsTer?
ENST00000498124.1:c.223_224delinsT	ENSP00000418915.1:p.Pro75SerfsTer?
ENST00000498628.6:c.70_71delinsT	ENSP00000467857.1:p.Pro24SerfsTer?
ENST00000530628.2:c.266_267delinsT	ENSP00000432664.2:p.Pro89LeufsTer?
ENST00000578845.2:c.70_71delinsT	ENSP00000467390.1:p.Pro24SerfsTer?
ENST00000579122.1:c.223_224delinsT	ENSP00000464202.1:p.Pro75SerfsTer?
ENST00000579755.1:c.266_267delinsT	ENSP00000462950.1:p.Pro89LeufsTer?
NM_000077.4:c.223_224delinsT , LRG_11t1:c.223_224delinsT	NP_000068.1:p.Pro75SerfsTer?
NM_001195132.1:c.223_224delinsT	NP_001182061.1:p.Pro75SerfsTer?
NM_058195.3:c.266_267delinsT , LRG_11t2:c.266_267delinsT	NP_478102.2:p.Pro89LeufsTer?
NM_058197.4:c.497_498delinsT	NP_478104.2:n.497_498delinsT
XM_005251343.1:c.70_71delinsT	XP_005251400.1:p.Pro24SerfsTer?
XM_011517675.1:c.223_224delinsT	XP_011515977.1:p.Pro75SerfsTer?
XM_011517676.1:c.223_224delinsT	XP_011515978.1:p.Pro75SerfsTer?
XM_011517679.1:c.70_71delinsT	XP_011515981.1:p.Pro24SerfsTer?
XR_929159.1:n.624_625delinsT
XR_929161.1:n.413_414delinsT
XR_929162.1:n.413_414delinsT
XR_929163.1:n.362_363delinsT
XR_929164.1:n.145_146delinsT
NM_001363763.1:c.70_71delinsT	NP_001350692.1:p.Pro24SerfsTer?
XM_011517675.2:c.223_224delinsT	XP_011515977.1:p.Pro75SerfsTer?
XM_011517676.2:c.223_224delinsT	XP_011515978.1:p.Pro75SerfsTer?
XR_929159.2:n.553_554delinsT
NM_001363763.2:c.70_71delinsT	NP_001350692.1:p.Pro24SerfsTer?
NM_000077.5:c.223_224delinsT MANE Select	NP_000068.1:p.Pro75SerfsTer?
NM_001195132.2:c.223_224delinsT	NP_001182061.1:p.Pro75SerfsTer?
NM_058195.4:c.266_267delinsT MANE Plus Clinical	NP_478102.2:p.Pro89LeufsTer?
NM_058197.5:c.*146_*147delinsT	NP_478104.2:n.*146_*147delinsT