Canonical Allele Identifier: CA645552558

Gene: CDKN2A

Linked Data

• COSMIC: COSM12531

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21971186_21971187insCCCCTCC , CM000671.2:g.21971186_21971187insCCCCTCC	GRCh38
NC_000009.11:g.21971185_21971186insCCCCTCC , CM000671.1:g.21971185_21971186insCCCCTCC	GRCh37
NC_000009.10:g.21961185_21961186insCCCCTCC	NCBI36
NG_007485.1:g.28306_28307insGAGGGGG , LRG_11:g.28306_28307insGAGGGGG

Transcript Alleles

HGVS	Amino-acid change
ENST00000304494.10:c.173_174insGAGGGGG MANE Select	ENSP00000307101.5:p.Val59ArgfsTer?
ENST00000404796.3:c.348-58247_348-58246insCCCCTCC	ENSP00000385916.2:n.348-58247_348-58246in...
ENST00000579755.2:c.216_217insGAGGGGG MANE Plus Clinical	ENSP00000462950.1:p.Ser73GlufsTer?
ENST00000304494.9:c.173_174insGAGGGGG	ENSP00000307101.5:p.Val59ArgfsTer?
ENST00000361570.4:c.216_217insGAGGGGG	ENSP00000355153.4:p.Ser73GlufsTer?
ENST00000380150.2:n.147_148insGAGGGGG
ENST00000380151.3:c.447_448insGAGGGGG	ENSP00000369496.3:n.447_448insGAGGGGG
ENST00000404796.2:c.348-58247_348-58246insCCCCTCC	ENSP00000385916.2:n.348-58247_348-58246in...
ENST00000479692.2:c.20_21insGAGGGGG	ENSP00000466887.1:p.Val8ArgfsTer?
ENST00000494262.5:c.20_21insGAGGGGG	ENSP00000464952.1:p.Val8ArgfsTer?
ENST00000497750.1:c.20_21insGAGGGGG	ENSP00000468510.1:p.Val8ArgfsTer?
ENST00000498124.1:c.173_174insGAGGGGG	ENSP00000418915.1:p.Val59ArgfsTer?
ENST00000498628.6:c.20_21insGAGGGGG	ENSP00000467857.1:p.Val8ArgfsTer?
ENST00000530628.2:c.216_217insGAGGGGG	ENSP00000432664.2:p.Ser73GlufsTer?
ENST00000578845.2:c.20_21insGAGGGGG	ENSP00000467390.1:p.Val8ArgfsTer?
ENST00000579122.1:c.173_174insGAGGGGG	ENSP00000464202.1:p.Val59ArgfsTer?
ENST00000579755.1:c.216_217insGAGGGGG	ENSP00000462950.1:p.Ser73GlufsTer?
NM_000077.4:c.173_174insGAGGGGG , LRG_11t1:c.173_174insGAGGGGG	NP_000068.1:p.Val59ArgfsTer?
NM_001195132.1:c.173_174insGAGGGGG	NP_001182061.1:p.Val59ArgfsTer?
NM_058195.3:c.216_217insGAGGGGG , LRG_11t2:c.216_217insGAGGGGG	NP_478102.2:p.Ser73GlufsTer?
NM_058197.4:c.447_448insGAGGGGG	NP_478104.2:n.447_448insGAGGGGG
XM_005251343.1:c.20_21insGAGGGGG	XP_005251400.1:p.Val8ArgfsTer?
XM_011517675.1:c.173_174insGAGGGGG	XP_011515977.1:p.Val59ArgfsTer?
XM_011517676.1:c.173_174insGAGGGGG	XP_011515978.1:p.Val59ArgfsTer?
XM_011517679.1:c.20_21insGAGGGGG	XP_011515981.1:p.Val8ArgfsTer?
XR_929159.1:n.574_575insGAGGGGG
XR_929161.1:n.363_364insGAGGGGG
XR_929162.1:n.363_364insGAGGGGG
XR_929163.1:n.312_313insGAGGGGG
XR_929164.1:n.95_96insGAGGGGG
NM_001363763.1:c.20_21insGAGGGGG	NP_001350692.1:p.Val8ArgfsTer?
XM_011517675.2:c.173_174insGAGGGGG	XP_011515977.1:p.Val59ArgfsTer?
XM_011517676.2:c.173_174insGAGGGGG	XP_011515978.1:p.Val59ArgfsTer?
XR_929159.2:n.503_504insGAGGGGG
NM_001363763.2:c.20_21insGAGGGGG	NP_001350692.1:p.Val8ArgfsTer?
NM_000077.5:c.173_174insGAGGGGG MANE Select	NP_000068.1:p.Val59ArgfsTer?
NM_001195132.2:c.173_174insGAGGGGG	NP_001182061.1:p.Val59ArgfsTer?
NM_058195.4:c.216_217insGAGGGGG MANE Plus Clinical	NP_478102.2:p.Ser73GlufsTer?
NM_058197.5:c.*96_*97insGAGGGGG	NP_478104.2:n.*96_*97insGAGGGGG