Canonical Allele Identifier: CA1839178834
Gene: CDKN2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.21988877C= , CM000671.2:g.21988877C= GRCh38
NC_000009.11:g.21988876C= , CM000671.1:g.21988876C= GRCh37
NC_000009.10:g.21978876C= NCBI36
NG_007485.1:g.10615G= , LRG_11:g.10615G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000404796.3:c.348-40556C= ENSP00000385916.2:n.348-40556C=
ENST00000579755.2:c.193+5262G= MANE Plus Clinical ENSP00000462950.1:n.193+5262G=
ENST00000361570.4:c.193+5262G= ENSP00000355153.4:n.193+5262G=
ENST00000404796.2:c.348-40556C= ENSP00000385916.2:n.348-40556C=
ENST00000494262.5:c.-4+5005G= ENSP00000464952.1:n.-4+5005G=
ENST00000498628.6:c.-4+5944G= ENSP00000467857.1:n.-4+5944G=
ENST00000530628.2:c.193+5262G= ENSP00000432664.2:n.193+5262G=
ENST00000579755.1:c.193+5262G= ENSP00000462950.1:n.193+5262G=
NM_058195.3:c.193+5262G= , LRG_11t2:c.193+5262G= NP_478102.2:n.193+5262G=
XM_011517678.1:c.*1053G= XP_011515980.1:n.*1053G=
XM_011517679.1:c.-4+5944G= XP_011515981.1:n.-4+5944G=
XR_929161.1:n.340+5262G=
XR_929162.1:n.340+5262G=
XR_929163.1:n.289+5262G=
NM_001363763.1:c.-4+5944G= NP_001350692.1:n.-4+5944G=
NM_001363763.2:c.-4+5944G= NP_001350692.1:n.-4+5944G=
NM_058195.4:c.193+5262G= MANE Plus Clinical NP_478102.2:n.193+5262G=