Canonical Allele Identifier: CA918426536

Gene: CDKN2A

Linked Data

• dbSNP Id: rs1554654057

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21971082_21971102del , CM000671.2:g.21971082_21971102del	GRCh38
NC_000009.11:g.21971081_21971101del , CM000671.1:g.21971081_21971101del	GRCh37
NC_000009.10:g.21961081_21961101del	NCBI36
NG_007485.1:g.28391_28411del , LRG_11:g.28391_28411del

Transcript Alleles

HGVS	Amino-acid change
ENST00000304494.10:c.258_278del MANE Select	ENSP00000307101.5:p.Arg87_Thr93del
ENST00000404796.3:c.348-58351_348-58331del	ENSP00000385916.2:n.348-58351_348-58331de...
ENST00000579755.2:c.301_321del MANE Plus Clinical	ENSP00000462950.1:p.Pro101_His107del
ENST00000304494.9:c.258_278del	ENSP00000307101.5:p.Arg87_Thr93del
ENST00000361570.4:c.300_320del	ENSP00000355153.4:p.Arg101_Thr107del
ENST00000380150.2:n.232_252del
ENST00000380151.3:c.532_552del	ENSP00000369496.3:n.532_552del
ENST00000404796.2:c.348-58351_348-58331del	ENSP00000385916.2:n.348-58351_348-58331de...
ENST00000479692.2:c.105_125del	ENSP00000466887.1:p.Arg36_Thr42del
ENST00000494262.5:c.105_125del	ENSP00000464952.1:p.Arg36_Thr42del
ENST00000497750.1:c.105_125del	ENSP00000468510.1:p.Arg36_Thr42del
ENST00000498124.1:c.258_278del	ENSP00000418915.1:p.Arg87_Thr93del
ENST00000498628.6:c.105_125del	ENSP00000467857.1:p.Arg36_Thr42del
ENST00000530628.2:c.301_321del	ENSP00000432664.2:p.Pro101_His107del
ENST00000578845.2:c.105_125del	ENSP00000467390.1:p.Arg36_Thr42del
ENST00000579122.1:c.258_278del	ENSP00000464202.1:p.Arg87_Thr93del
ENST00000579755.1:c.301_321del	ENSP00000462950.1:p.Pro101_His107del
NM_000077.4:c.258_278del , LRG_11t1:c.258_278del	NP_000068.1:p.Arg87_Thr93del
NM_001195132.1:c.258_278del	NP_001182061.1:p.Arg87_Thr93del
NM_058195.3:c.301_321del , LRG_11t2:c.301_321del	NP_478102.2:p.Pro101_His107del
NM_058197.4:c.532_552del	NP_478104.2:n.532_552del
XM_005251343.1:c.105_125del	XP_005251400.1:p.Arg36_Thr42del
XM_011517675.1:c.258_278del	XP_011515977.1:p.Arg87_Thr93del
XM_011517676.1:c.258_278del	XP_011515978.1:p.Arg87_Thr93del
XM_011517679.1:c.105_125del	XP_011515981.1:p.Arg36_Thr42del
XR_929159.1:n.659_679del
XR_929161.1:n.448_468del
XR_929162.1:n.448_468del
XR_929163.1:n.397_417del
XR_929164.1:n.180_200del
NM_001363763.1:c.105_125del	NP_001350692.1:p.Arg36_Thr42del
XM_011517675.2:c.258_278del	XP_011515977.1:p.Arg87_Thr93del
XM_011517676.2:c.258_278del	XP_011515978.1:p.Arg87_Thr93del
XR_929159.2:n.588_608del
NM_001363763.2:c.105_125del	NP_001350692.1:p.Arg36_Thr42del
NM_000077.5:c.258_278del MANE Select	NP_000068.1:p.Arg87_Thr93del
NM_001195132.2:c.258_278del	NP_001182061.1:p.Arg87_Thr93del
NM_058195.4:c.301_321del MANE Plus Clinical	NP_478102.2:p.Pro101_His107del
NM_058197.5:c.*181_*201del	NP_478104.2:n.*181_*201del