Canonical Allele Identifier: CA645552557
Gene: CDKN2A HGNC NCBI

Linked Data

COSMIC: COSM13494

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.21971187_21971200del , CM000671.2:g.21971187_21971200del GRCh38
NC_000009.11:g.21971186_21971199del , CM000671.1:g.21971186_21971199del GRCh37
NC_000009.10:g.21961186_21961199del NCBI36
NG_007485.1:g.28294_28307del , LRG_11:g.28294_28307del

Transcript Alleles

HGVS Amino-acid Change
ENST00000304494.10:c.161_174del MANE Select ENSP00000307101.5:p.Met54SerfsTer?
ENST00000404796.3:c.348-58246_348-58233del ENSP00000385916.2:n.348-58246_348-58233del
ENST00000579755.2:c.204_217del MANE Plus Clinical ENSP00000462950.1:p.Asp68GlufsTer?
ENST00000304494.9:c.161_174del ENSP00000307101.5:p.Met54SerfsTer?
ENST00000361570.4:c.204_217del ENSP00000355153.4:p.Asp68GlufsTer?
ENST00000380150.2:n.135_148del
ENST00000380151.3:c.435_448del ENSP00000369496.3:n.435_448del
ENST00000404796.2:c.348-58246_348-58233del ENSP00000385916.2:n.348-58246_348-58233del
ENST00000479692.2:c.8_21del ENSP00000466887.1:p.Met3SerfsTer?
ENST00000494262.5:c.8_21del ENSP00000464952.1:p.Met3SerfsTer?
ENST00000497750.1:c.8_21del ENSP00000468510.1:p.Met3SerfsTer?
ENST00000498124.1:c.161_174del ENSP00000418915.1:p.Met54SerfsTer?
ENST00000498628.6:c.8_21del ENSP00000467857.1:p.Met3SerfsTer?
ENST00000530628.2:c.204_217del ENSP00000432664.2:p.Asp68GlufsTer?
ENST00000578845.2:c.8_21del ENSP00000467390.1:p.Met3SerfsTer?
ENST00000579122.1:c.161_174del ENSP00000464202.1:p.Met54SerfsTer?
ENST00000579755.1:c.204_217del ENSP00000462950.1:p.Asp68GlufsTer?
NM_000077.4:c.161_174del , LRG_11t1:c.161_174del NP_000068.1:p.Met54SerfsTer?
NM_001195132.1:c.161_174del NP_001182061.1:p.Met54SerfsTer?
NM_058195.3:c.204_217del , LRG_11t2:c.204_217del NP_478102.2:p.Asp68GlufsTer?
NM_058197.4:c.435_448del NP_478104.2:n.435_448del
XM_005251343.1:c.8_21del XP_005251400.1:p.Met3SerfsTer?
XM_011517675.1:c.161_174del XP_011515977.1:p.Met54SerfsTer?
XM_011517676.1:c.161_174del XP_011515978.1:p.Met54SerfsTer?
XM_011517679.1:c.8_21del XP_011515981.1:p.Met3SerfsTer?
XR_929159.1:n.562_575del
XR_929161.1:n.351_364del
XR_929162.1:n.351_364del
XR_929163.1:n.300_313del
XR_929164.1:n.83_96del
NM_001363763.1:c.8_21del NP_001350692.1:p.Met3SerfsTer?
XM_011517675.2:c.161_174del XP_011515977.1:p.Met54SerfsTer?
XM_011517676.2:c.161_174del XP_011515978.1:p.Met54SerfsTer?
XR_929159.2:n.491_504del
NM_001363763.2:c.8_21del NP_001350692.1:p.Met3SerfsTer?
NM_000077.5:c.161_174del MANE Select NP_000068.1:p.Met54SerfsTer?
NM_001195132.2:c.161_174del NP_001182061.1:p.Met54SerfsTer?
NM_058195.4:c.204_217del MANE Plus Clinical NP_478102.2:p.Asp68GlufsTer?
NM_058197.5:c.*84_*97del NP_478104.2:n.*84_*97del