Canonical Allele Identifier: CA464261853

Gene: CDKN2A

Linked Data

• MyVariant Identifiers: chr9:g.21971183_21971184insG (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21971184_21971185insG , CM000671.2:g.21971184_21971185insG	GRCh38
NC_000009.11:g.21971183_21971184insG , CM000671.1:g.21971183_21971184insG	GRCh37
NC_000009.10:g.21961183_21961184insG	NCBI36
NG_007485.1:g.28307_28308insC , LRG_11:g.28307_28308insC

Transcript Alleles

HGVS	Amino-acid change
ENST00000304494.10:c.174_175insC MANE Select	ENSP00000307101.5:p.Val59ArgfsTer?
ENST00000404796.3:c.348-58249_348-58248insG	ENSP00000385916.2:n.348-58249_348-58248in...
ENST00000579755.2:c.217_218insC MANE Plus Clinical	ENSP00000462950.1:p.Ser73ThrfsTer?
ENST00000304494.9:c.174_175insC	ENSP00000307101.5:p.Val59ArgfsTer?
ENST00000361570.4:c.217_218insC	ENSP00000355153.4:p.Ser73ThrfsTer?
ENST00000380150.2:n.148_149insC
ENST00000380151.3:c.448_449insC	ENSP00000369496.3:n.448_449insC
ENST00000404796.2:c.348-58249_348-58248insG	ENSP00000385916.2:n.348-58249_348-58248in...
ENST00000479692.2:c.21_22insC	ENSP00000466887.1:p.Val8ArgfsTer?
ENST00000494262.5:c.21_22insC	ENSP00000464952.1:p.Val8ArgfsTer?
ENST00000497750.1:c.21_22insC	ENSP00000468510.1:p.Val8ArgfsTer?
ENST00000498124.1:c.174_175insC	ENSP00000418915.1:p.Val59ArgfsTer?
ENST00000498628.6:c.21_22insC	ENSP00000467857.1:p.Val8ArgfsTer?
ENST00000530628.2:c.217_218insC	ENSP00000432664.2:p.Ser73ThrfsTer?
ENST00000578845.2:c.21_22insC	ENSP00000467390.1:p.Val8ArgfsTer?
ENST00000579122.1:c.174_175insC	ENSP00000464202.1:p.Val59ArgfsTer?
ENST00000579755.1:c.217_218insC	ENSP00000462950.1:p.Ser73ThrfsTer?
NM_000077.4:c.174_175insC , LRG_11t1:c.174_175insC	NP_000068.1:p.Val59ArgfsTer?
NM_001195132.1:c.174_175insC	NP_001182061.1:p.Val59ArgfsTer?
NM_058195.3:c.217_218insC , LRG_11t2:c.217_218insC	NP_478102.2:p.Ser73ThrfsTer?
NM_058197.4:c.448_449insC	NP_478104.2:n.448_449insC
XM_005251343.1:c.21_22insC	XP_005251400.1:p.Val8ArgfsTer?
XM_011517675.1:c.174_175insC	XP_011515977.1:p.Val59ArgfsTer?
XM_011517676.1:c.174_175insC	XP_011515978.1:p.Val59ArgfsTer?
XM_011517679.1:c.21_22insC	XP_011515981.1:p.Val8ArgfsTer?
XR_929159.1:n.575_576insC
XR_929161.1:n.364_365insC
XR_929162.1:n.364_365insC
XR_929163.1:n.313_314insC
XR_929164.1:n.96_97insC
NM_001363763.1:c.21_22insC	NP_001350692.1:p.Val8ArgfsTer?
XM_011517675.2:c.174_175insC	XP_011515977.1:p.Val59ArgfsTer?
XM_011517676.2:c.174_175insC	XP_011515978.1:p.Val59ArgfsTer?
XR_929159.2:n.504_505insC
NM_001363763.2:c.21_22insC	NP_001350692.1:p.Val8ArgfsTer?
NM_000077.5:c.174_175insC MANE Select	NP_000068.1:p.Val59ArgfsTer?
NM_001195132.2:c.174_175insC	NP_001182061.1:p.Val59ArgfsTer?
NM_058195.4:c.217_218insC MANE Plus Clinical	NP_478102.2:p.Ser73ThrfsTer?
NM_058197.5:c.*97_*98insC	NP_478104.2:n.*97_*98insC