Canonical Allele Identifier: CA2689599466
Gene: CDKN2A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.21975028_21975056del , CM000671.2:g.21975028_21975056del GRCh38
NC_000009.11:g.21975027_21975055del , CM000671.1:g.21975027_21975055del GRCh37
NC_000009.10:g.21965027_21965055del NCBI36
NG_007485.1:g.24440_24468del , LRG_11:g.24440_24468del

Transcript Alleles

HGVS Amino-acid Change
ENST00000404796.3:c.348-54405_348-54377del ENSP00000385916.2:n.348-54405_348-54377del
ENST00000579755.2:c.194-3844_194-3816del MANE Plus Clinical ENSP00000462950.1:n.194-3844_194-3816del
ENST00000304494.9:c.-225_-197del ENSP00000307101.5:n.-225_-197del
ENST00000361570.4:c.194-3844_194-3816del ENSP00000355153.4:n.194-3844_194-3816del
ENST00000404796.2:c.348-54405_348-54377del ENSP00000385916.2:n.348-54405_348-54377del
ENST00000494262.5:c.-3-3844_-3-3816del ENSP00000464952.1:n.-3-3844_-3-3816del
ENST00000498628.6:c.-3-3844_-3-3816del ENSP00000467857.1:n.-3-3844_-3-3816del
ENST00000530628.2:c.194-3844_194-3816del ENSP00000432664.2:n.194-3844_194-3816del
ENST00000579755.1:c.194-3844_194-3816del ENSP00000462950.1:n.194-3844_194-3816del
NM_000077.4:c.-225_-197del , LRG_11t1:c.-225_-197del NP_000068.1:n.-225_-197del
NM_001195132.1:c.-225_-197del NP_001182061.1:n.-225_-197del
NM_058195.3:c.194-3844_194-3816del , LRG_11t2:c.194-3844_194-3816del NP_478102.2:n.194-3844_194-3816del
XM_011517675.1:c.-225_-197del XP_011515977.1:n.-225_-197del
XM_011517676.1:c.-225_-197del XP_011515978.1:n.-225_-197del
XM_011517679.1:c.-3-3844_-3-3816del XP_011515981.1:n.-3-3844_-3-3816del
XR_929159.1:n.177_205del
XR_929161.1:n.341-3844_341-3816del
XR_929162.1:n.341-3844_341-3816del
XR_929163.1:n.290-3844_290-3816del
NM_001363763.1:c.-3-3844_-3-3816del NP_001350692.1:n.-3-3844_-3-3816del
XM_011517675.2:c.-225_-197del XP_011515977.1:n.-225_-197del
XM_011517676.2:c.-225_-197del XP_011515978.1:n.-225_-197del
XR_929159.2:n.106_134del
NM_001363763.2:c.-3-3844_-3-3816del NP_001350692.1:n.-3-3844_-3-3816del
NM_058195.4:c.194-3844_194-3816del MANE Plus Clinical NP_478102.2:n.194-3844_194-3816del