Canonical Allele Identifier: CA2573143730

Gene: CDKN2A

Linked Data

• dbSNP Id: rs2131094214

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21971063_21971074del , CM000671.2:g.21971063_21971074del	GRCh38
NC_000009.11:g.21971062_21971073del , CM000671.1:g.21971062_21971073del	GRCh37
NC_000009.10:g.21961062_21961073del	NCBI36
NG_007485.1:g.28420_28431del , LRG_11:g.28420_28431del

Transcript Alleles

HGVS	Amino-acid change
ENST00000304494.10:c.287_298del MANE Select	ENSP00000307101.5:p.Val96_Arg99del
ENST00000404796.3:c.348-58370_348-58359del	ENSP00000385916.2:n.348-58370_348-58359del
ENST00000579755.2:c.330_341del MANE Plus Clinical	ENSP00000462950.1:p.Ala111_Gly114del
ENST00000304494.9:c.287_298del	ENSP00000307101.5:p.Val96_Arg99del
ENST00000361570.4:c.329_340del	ENSP00000355153.4:p.Val110_Arg113del
ENST00000380150.2:n.261_272del
ENST00000380151.3:c.561_572del	ENSP00000369496.3:n.561_572del
ENST00000404796.2:c.348-58370_348-58359del	ENSP00000385916.2:n.348-58370_348-58359del
ENST00000479692.2:c.134_145del	ENSP00000466887.1:p.Val45_Arg48del
ENST00000494262.5:c.134_145del	ENSP00000464952.1:p.Val45_Arg48del
ENST00000497750.1:c.134_145del	ENSP00000468510.1:p.Val45_Arg48del
ENST00000498124.1:c.287_298del	ENSP00000418915.1:p.Val96_Arg99del
ENST00000498628.6:c.134_145del	ENSP00000467857.1:p.Val45_Arg48del
ENST00000530628.2:c.330_341del	ENSP00000432664.2:p.Ala111_Gly114del
ENST00000578845.2:c.134_145del	ENSP00000467390.1:p.Val45_Arg48del
ENST00000579122.1:c.287_298del	ENSP00000464202.1:p.Val96_Arg99del
ENST00000579755.1:c.330_341del	ENSP00000462950.1:p.Ala111_Gly114del
NM_000077.4:c.287_298del , LRG_11t1:c.287_298del	NP_000068.1:p.Val96_Arg99del
NM_001195132.1:c.287_298del	NP_001182061.1:p.Val96_Arg99del
NM_058195.3:c.330_341del , LRG_11t2:c.330_341del	NP_478102.2:p.Ala111_Gly114del
NM_058197.4:c.561_572del	NP_478104.2:n.561_572del
XM_005251343.1:c.134_145del	XP_005251400.1:p.Val45_Arg48del
XM_011517675.1:c.287_298del	XP_011515977.1:p.Val96_Arg99del
XM_011517676.1:c.287_298del	XP_011515978.1:p.Val96_Arg99del
XM_011517679.1:c.134_145del	XP_011515981.1:p.Val45_Arg48del
XR_929159.1:n.688_699del
XR_929161.1:n.477_488del
XR_929162.1:n.477_488del
XR_929163.1:n.426_437del
XR_929164.1:n.209_220del
NM_001363763.1:c.134_145del	NP_001350692.1:p.Val45_Arg48del
XM_011517675.2:c.287_298del	XP_011515977.1:p.Val96_Arg99del
XM_011517676.2:c.287_298del	XP_011515978.1:p.Val96_Arg99del
XR_929159.2:n.617_628del
NM_001363763.2:c.134_145del	NP_001350692.1:p.Val45_Arg48del
NM_000077.5:c.287_298del MANE Select	NP_000068.1:p.Val96_Arg99del
NM_001195132.2:c.287_298del	NP_001182061.1:p.Val96_Arg99del
NM_058195.4:c.330_341del MANE Plus Clinical	NP_478102.2:p.Ala111_Gly114del
NM_058197.5:c.*210_*221del	NP_478104.2:n.*210_*221del