Canonical Allele Identifier: CA1839171987
Gene: CDKN2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.21974226_21974230delinsATATT , CM000671.2:g.21974226_21974230delinsATATT GRCh38
NC_000009.11:g.21974225_21974229delinsATATT , CM000671.1:g.21974225_21974229delinsATATT GRCh37
NC_000009.10:g.21964225_21964229delinsATATT NCBI36
NG_007485.1:g.25262_25266delinsAATAT , LRG_11:g.25262_25266delinsAATAT

Transcript Alleles

HGVS Amino-acid change
ENST00000304494.10:c.150+448_150+452delinsAATAT MANE Select ENSP00000307101.5:n.150+448_150+452delins...
ENST00000404796.3:c.348-55207_348-55203delinsATATT ENSP00000385916.2:n.348-55207_348-55203de...
ENST00000579755.2:c.194-3022_194-3018delinsAATAT MANE Plus Clinical ENSP00000462950.1:n.194-3022_194-3018deli...
ENST00000304494.9:c.150+448_150+452delinsAATAT ENSP00000307101.5:n.150+448_150+452delins...
ENST00000361570.4:c.194-3022_194-3018delinsAATAT ENSP00000355153.4:n.194-3022_194-3018deli...
ENST00000380151.3:c.424+174_424+178delinsAATAT ENSP00000369496.3:n.424+174_424+178delins...
ENST00000404796.2:c.348-55207_348-55203delinsATATT ENSP00000385916.2:n.348-55207_348-55203de...
ENST00000494262.5:c.-3-3022_-3-3018delinsAATAT ENSP00000464952.1:n.-3-3022_-3-3018delins...
ENST00000498124.1:c.150+448_150+452delinsAATAT ENSP00000418915.1:n.150+448_150+452delins...
ENST00000498628.6:c.-3-3022_-3-3018delinsAATAT ENSP00000467857.1:n.-3-3022_-3-3018delins...
ENST00000530628.2:c.194-3022_194-3018delinsAATAT ENSP00000432664.2:n.194-3022_194-3018deli...
ENST00000579122.1:c.150+448_150+452delinsAATAT ENSP00000464202.1:n.150+448_150+452delins...
ENST00000579755.1:c.194-3022_194-3018delinsAATAT ENSP00000462950.1:n.194-3022_194-3018deli...
NM_000077.4:c.150+448_150+452delinsAATAT , LRG_11t1:c.150+448_150+452delinsAATAT NP_000068.1:n.150+448_150+452delinsAATAT
NM_001195132.1:c.150+448_150+452delinsAATAT NP_001182061.1:n.150+448_150+452delinsAAT...
NM_058195.3:c.194-3022_194-3018delinsAATAT , LRG_11t2:c.194-3022_194-3018delinsAATAT NP_478102.2:n.194-3022_194-3018delinsAATA...
NM_058197.4:c.424+174_424+178delinsAATAT NP_478104.2:n.424+174_424+178delinsAATAT
XM_011517675.1:c.150+448_150+452delinsAATAT XP_011515977.1:n.150+448_150+452delinsAAT...
XM_011517676.1:c.150+448_150+452delinsAATAT XP_011515978.1:n.150+448_150+452delinsAAT...
XM_011517679.1:c.-3-3022_-3-3018delinsAATAT XP_011515981.1:n.-3-3022_-3-3018delinsAAT...
XR_929159.1:n.551+448_551+452delinsAATAT
XR_929161.1:n.341-3022_341-3018delinsAATAT
XR_929162.1:n.341-3022_341-3018delinsAATAT
XR_929163.1:n.290-3022_290-3018delinsAATAT
NM_001363763.1:c.-3-3022_-3-3018delinsAATAT NP_001350692.1:n.-3-3022_-3-3018delinsAAT...
XM_011517675.2:c.150+448_150+452delinsAATAT XP_011515977.1:n.150+448_150+452delinsAAT...
XM_011517676.2:c.150+448_150+452delinsAATAT XP_011515978.1:n.150+448_150+452delinsAAT...
XR_929159.2:n.480+448_480+452delinsAATAT
NM_001363763.2:c.-3-3022_-3-3018delinsAATAT NP_001350692.1:n.-3-3022_-3-3018delinsAAT...
NM_000077.5:c.150+448_150+452delinsAATAT MANE Select NP_000068.1:n.150+448_150+452delinsAATAT
NM_001195132.2:c.150+448_150+452delinsAATAT NP_001182061.1:n.150+448_150+452delinsAAT...
NM_058195.4:c.194-3022_194-3018delinsAATAT MANE Plus Clinical NP_478102.2:n.194-3022_194-3018delinsAATA...
NM_058197.5:c.*73+174_*73+178delinsAATAT NP_478104.2:n.*73+174_*73+178delinsAATAT