Canonical Allele Identifier: CA1839160490
Gene: CDKN2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.21970797A= , CM000671.2:g.21970797A= GRCh38
NC_000009.11:g.21970796A= , CM000671.1:g.21970796A= GRCh37
NC_000009.10:g.21960796A= NCBI36
NG_007485.1:g.28695T= , LRG_11:g.28695T=

Transcript Alleles

HGVS Amino-acid change
ENST00000304494.10:c.457+105T= MANE Select ENSP00000307101.5:n.457+105T=
ENST00000404796.3:c.348-58636A= ENSP00000385916.2:n.348-58636A=
ENST00000579755.2:c.*101+105T= MANE Plus Clinical ENSP00000462950.1:n.*101+105T=
ENST00000304494.9:c.457+105T= ENSP00000307101.5:n.457+105T=
ENST00000361570.4:c.499+105T= ENSP00000355153.4:n.499+105T=
ENST00000380150.2:n.431+105T=
ENST00000380151.3:c.731+105T= ENSP00000369496.3:n.731+105T=
ENST00000404796.2:c.348-58636A= ENSP00000385916.2:n.348-58636A=
ENST00000479692.2:c.304+105T= ENSP00000466887.1:n.304+105T=
ENST00000494262.5:c.304+105T= ENSP00000464952.1:n.304+105T=
ENST00000497750.1:c.*94T= ENSP00000468510.1:n.*94T=
ENST00000498124.1:c.457+105T= ENSP00000418915.1:n.457+105T=
ENST00000498628.6:c.304+105T= ENSP00000467857.1:n.304+105T=
ENST00000530628.2:c.*27+179T= ENSP00000432664.2:n.*27+179T=
ENST00000578845.2:c.304+105T= ENSP00000467390.1:n.304+105T=
ENST00000579122.1:c.383+179T= ENSP00000464202.1:n.383+179T=
ENST00000579755.1:c.*101+105T= ENSP00000462950.1:n.*101+105T=
NM_000077.4:c.457+105T= , LRG_11t1:c.457+105T= NP_000068.1:n.457+105T=
NM_001195132.1:c.457+105T= NP_001182061.1:n.457+105T=
NM_058195.3:c.*101+105T= , LRG_11t2:c.*101+105T= NP_478102.2:n.*101+105T=
NM_058197.4:c.731+105T= NP_478104.2:n.731+105T=
XM_005251343.1:c.304+105T= XP_005251400.1:n.304+105T=
XM_011517675.1:c.457+105T= XP_011515977.1:n.457+105T=
XM_011517676.1:c.457+105T= XP_011515978.1:n.457+105T=
XM_011517679.1:c.304+105T= XP_011515981.1:n.304+105T=
XR_929159.1:n.858+105T=
XR_929161.1:n.647+105T=
XR_929162.1:n.647+105T=
XR_929163.1:n.596+105T=
XR_929164.1:n.379+105T=
NM_001363763.1:c.304+105T= NP_001350692.1:n.304+105T=
XM_011517675.2:c.457+105T= XP_011515977.1:n.457+105T=
XM_011517676.2:c.457+105T= XP_011515978.1:n.457+105T=
XR_929159.2:n.787+105T=
NM_001363763.2:c.304+105T= NP_001350692.1:n.304+105T=
NM_000077.5:c.457+105T= MANE Select NP_000068.1:n.457+105T=
NM_001195132.2:c.457+105T= NP_001182061.1:n.457+105T=
NM_058195.4:c.*101+105T= MANE Plus Clinical NP_478102.2:n.*101+105T=
NM_058197.5:c.*380+105T= NP_478104.2:n.*380+105T=