Canonical Allele Identifier: CA1839160616
Gene: CDKN2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.21970902C= , CM000671.2:g.21970902C= GRCh38
NC_000009.11:g.21970901C= , CM000671.1:g.21970901C= GRCh37
NC_000009.10:g.21960901C= NCBI36
NG_007485.1:g.28590G= , LRG_11:g.28590G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000304494.10:c.457G= MANE Select ENSP00000307101.5:p.Asp153=
ENST00000404796.3:c.348-58531C= ENSP00000385916.2:n.348-58531C=
ENST00000579755.2:c.*101G= MANE Plus Clinical ENSP00000462950.1:n.*101G=
ENST00000304494.9:c.457G= ENSP00000307101.5:p.Asp153=
ENST00000361570.4:c.499G= ENSP00000355153.4:p.Asp167=
ENST00000380150.2:n.431G=
ENST00000380151.3:c.731G= ENSP00000369496.3:n.731G=
ENST00000404796.2:c.348-58531C= ENSP00000385916.2:n.348-58531C=
ENST00000479692.2:c.304G= ENSP00000466887.1:p.Val102=
ENST00000494262.5:c.304G= ENSP00000464952.1:p.Asp102=
ENST00000497750.1:c.304G= ENSP00000468510.1:p.Gly102=
ENST00000498124.1:c.457G= ENSP00000418915.1:p.Glu153=
ENST00000498628.6:c.304G= ENSP00000467857.1:p.Asp102=
ENST00000530628.2:c.*27+74G= ENSP00000432664.2:n.*27+74G=
ENST00000578845.2:c.304G= ENSP00000467390.1:p.Asp102=
ENST00000579122.1:c.383+74G= ENSP00000464202.1:n.383+74G=
ENST00000579755.1:c.*101G= ENSP00000462950.1:n.*101G=
NM_000077.4:c.457G= , LRG_11t1:c.457G= NP_000068.1:p.Asp153=
NM_001195132.1:c.457G= NP_001182061.1:p.Glu153=
NM_058195.3:c.*101G= , LRG_11t2:c.*101G= NP_478102.2:n.*101G=
NM_058197.4:c.731G= NP_478104.2:n.731G=
XM_005251343.1:c.304G= XP_005251400.1:p.Asp102=
XM_011517675.1:c.457G= XP_011515977.1:p.Ala153=
XM_011517676.1:c.457G= XP_011515978.1:p.Val153=
XM_011517679.1:c.304G= XP_011515981.1:p.Asp102=
XR_929159.1:n.858G=
XR_929161.1:n.647G=
XR_929162.1:n.647G=
XR_929163.1:n.596G=
XR_929164.1:n.379G=
NM_001363763.1:c.304G= NP_001350692.1:p.Asp102=
XM_011517675.2:c.457G= XP_011515977.1:p.Ala153=
XM_011517676.2:c.457G= XP_011515978.1:p.Val153=
XR_929159.2:n.787G=
NM_001363763.2:c.304G= NP_001350692.1:p.Asp102=
NM_000077.5:c.457G= MANE Select NP_000068.1:p.Asp153=
NM_001195132.2:c.457G= NP_001182061.1:p.Glu153=
NM_058195.4:c.*101G= MANE Plus Clinical NP_478102.2:n.*101G=
NM_058197.5:c.*380G= NP_478104.2:n.*380G=