Canonical Allele Identifier: CA1839178831
Gene: CDKN2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.21988868G= , CM000671.2:g.21988868G= GRCh38
NC_000009.11:g.21988867G= , CM000671.1:g.21988867G= GRCh37
NC_000009.10:g.21978867G= NCBI36
NG_007485.1:g.10624C= , LRG_11:g.10624C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000404796.3:c.348-40565G= ENSP00000385916.2:n.348-40565G=
ENST00000579755.2:c.193+5271C= MANE Plus Clinical ENSP00000462950.1:n.193+5271C=
ENST00000361570.4:c.193+5271C= ENSP00000355153.4:n.193+5271C=
ENST00000404796.2:c.348-40565G= ENSP00000385916.2:n.348-40565G=
ENST00000494262.5:c.-4+5014C= ENSP00000464952.1:n.-4+5014C=
ENST00000498628.6:c.-4+5953C= ENSP00000467857.1:n.-4+5953C=
ENST00000530628.2:c.193+5271C= ENSP00000432664.2:n.193+5271C=
ENST00000579755.1:c.193+5271C= ENSP00000462950.1:n.193+5271C=
NM_058195.3:c.193+5271C= , LRG_11t2:c.193+5271C= NP_478102.2:n.193+5271C=
XM_011517678.1:c.*1062C= XP_011515980.1:n.*1062C=
XM_011517679.1:c.-4+5953C= XP_011515981.1:n.-4+5953C=
XR_929161.1:n.340+5271C=
XR_929162.1:n.340+5271C=
XR_929163.1:n.289+5271C=
NM_001363763.1:c.-4+5953C= NP_001350692.1:n.-4+5953C=
NM_001363763.2:c.-4+5953C= NP_001350692.1:n.-4+5953C=
NM_058195.4:c.193+5271C= MANE Plus Clinical NP_478102.2:n.193+5271C=