Canonical Allele Identifier: CA1839161798

Gene: CDKN2A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21971099C= , CM000671.2:g.21971099C=	GRCh38
NC_000009.11:g.21971098C= , CM000671.1:g.21971098C=	GRCh37
NC_000009.10:g.21961098C=	NCBI36
NG_007485.1:g.28393G= , LRG_11:g.28393G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000304494.10:c.260G= MANE Select	ENSP00000307101.5:p.Arg87=
ENST00000404796.3:c.348-58334C=	ENSP00000385916.2:n.348-58334C=
ENST00000579755.2:c.303G= MANE Plus Clinical	ENSP00000462950.1:p.Pro101=
ENST00000304494.9:c.260G=	ENSP00000307101.5:p.Arg87=
ENST00000361570.4:c.302G=	ENSP00000355153.4:p.Arg101=
ENST00000380150.2:n.234G=
ENST00000380151.3:c.534G=	ENSP00000369496.3:n.534G=
ENST00000404796.2:c.348-58334C=	ENSP00000385916.2:n.348-58334C=
ENST00000479692.2:c.107G=	ENSP00000466887.1:p.Arg36=
ENST00000494262.5:c.107G=	ENSP00000464952.1:p.Arg36=
ENST00000497750.1:c.107G=	ENSP00000468510.1:p.Arg36=
ENST00000498124.1:c.260G=	ENSP00000418915.1:p.Arg87=
ENST00000498628.6:c.107G=	ENSP00000467857.1:p.Arg36=
ENST00000530628.2:c.303G=	ENSP00000432664.2:p.Pro101=
ENST00000578845.2:c.107G=	ENSP00000467390.1:p.Arg36=
ENST00000579122.1:c.260G=	ENSP00000464202.1:p.Arg87=
ENST00000579755.1:c.303G=	ENSP00000462950.1:p.Pro101=
NM_000077.4:c.260G= , LRG_11t1:c.260G=	NP_000068.1:p.Arg87=
NM_001195132.1:c.260G=	NP_001182061.1:p.Arg87=
NM_058195.3:c.303G= , LRG_11t2:c.303G=	NP_478102.2:p.Pro101=
NM_058197.4:c.534G=	NP_478104.2:n.534G=
XM_005251343.1:c.107G=	XP_005251400.1:p.Arg36=
XM_011517675.1:c.260G=	XP_011515977.1:p.Arg87=
XM_011517676.1:c.260G=	XP_011515978.1:p.Arg87=
XM_011517679.1:c.107G=	XP_011515981.1:p.Arg36=
XR_929159.1:n.661G=
XR_929161.1:n.450G=
XR_929162.1:n.450G=
XR_929163.1:n.399G=
XR_929164.1:n.182G=
NM_001363763.1:c.107G=	NP_001350692.1:p.Arg36=
XM_011517675.2:c.260G=	XP_011515977.1:p.Arg87=
XM_011517676.2:c.260G=	XP_011515978.1:p.Arg87=
XR_929159.2:n.590G=
NM_001363763.2:c.107G=	NP_001350692.1:p.Arg36=
NM_000077.5:c.260G= MANE Select	NP_000068.1:p.Arg87=
NM_001195132.2:c.260G=	NP_001182061.1:p.Arg87=
NM_058195.4:c.303G= MANE Plus Clinical	NP_478102.2:p.Pro101=
NM_058197.5:c.*183G=	NP_478104.2:n.*183G=