Canonical Allele Identifier: CA1839171887
Gene: CDKN2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.21974144_21974145delinsAT , CM000671.2:g.21974144_21974145delinsAT GRCh38
NC_000009.11:g.21974143_21974144delinsAT , CM000671.1:g.21974143_21974144delinsAT GRCh37
NC_000009.10:g.21964143_21964144delinsAT NCBI36
NG_007485.1:g.25347_25348delinsAT , LRG_11:g.25347_25348delinsAT

Transcript Alleles

HGVS Amino-acid change
ENST00000304494.10:c.150+533_150+534delinsAT MANE Select ENSP00000307101.5:n.150+533_150+534delins...
ENST00000404796.3:c.348-55289_348-55288delinsAT ENSP00000385916.2:n.348-55289_348-55288de...
ENST00000579755.2:c.194-2937_194-2936delinsAT MANE Plus Clinical ENSP00000462950.1:n.194-2937_194-2936deli...
ENST00000304494.9:c.150+533_150+534delinsAT ENSP00000307101.5:n.150+533_150+534delins...
ENST00000361570.4:c.194-2937_194-2936delinsAT ENSP00000355153.4:n.194-2937_194-2936deli...
ENST00000380151.3:c.424+259_424+260delinsAT ENSP00000369496.3:n.424+259_424+260delins...
ENST00000404796.2:c.348-55289_348-55288delinsAT ENSP00000385916.2:n.348-55289_348-55288de...
ENST00000494262.5:c.-3-2937_-3-2936delinsAT ENSP00000464952.1:n.-3-2937_-3-2936delins...
ENST00000498124.1:c.150+533_150+534delinsAT ENSP00000418915.1:n.150+533_150+534delins...
ENST00000498628.6:c.-3-2937_-3-2936delinsAT ENSP00000467857.1:n.-3-2937_-3-2936delins...
ENST00000530628.2:c.194-2937_194-2936delinsAT ENSP00000432664.2:n.194-2937_194-2936deli...
ENST00000579122.1:c.150+533_150+534delinsAT ENSP00000464202.1:n.150+533_150+534delins...
ENST00000579755.1:c.194-2937_194-2936delinsAT ENSP00000462950.1:n.194-2937_194-2936deli...
NM_000077.4:c.150+533_150+534delinsAT , LRG_11t1:c.150+533_150+534delinsAT NP_000068.1:n.150+533_150+534delinsAT
NM_001195132.1:c.150+533_150+534delinsAT NP_001182061.1:n.150+533_150+534delinsAT
NM_058195.3:c.194-2937_194-2936delinsAT , LRG_11t2:c.194-2937_194-2936delinsAT NP_478102.2:n.194-2937_194-2936delinsAT
NM_058197.4:c.424+259_424+260delinsAT NP_478104.2:n.424+259_424+260delinsAT
XM_011517675.1:c.150+533_150+534delinsAT XP_011515977.1:n.150+533_150+534delinsAT
XM_011517676.1:c.150+533_150+534delinsAT XP_011515978.1:n.150+533_150+534delinsAT
XM_011517679.1:c.-3-2937_-3-2936delinsAT XP_011515981.1:n.-3-2937_-3-2936delinsAT
XR_929159.1:n.551+533_551+534delinsAT
XR_929161.1:n.341-2937_341-2936delinsAT
XR_929162.1:n.341-2937_341-2936delinsAT
XR_929163.1:n.290-2937_290-2936delinsAT
NM_001363763.1:c.-3-2937_-3-2936delinsAT NP_001350692.1:n.-3-2937_-3-2936delinsAT
XM_011517675.2:c.150+533_150+534delinsAT XP_011515977.1:n.150+533_150+534delinsAT
XM_011517676.2:c.150+533_150+534delinsAT XP_011515978.1:n.150+533_150+534delinsAT
XR_929159.2:n.480+533_480+534delinsAT
NM_001363763.2:c.-3-2937_-3-2936delinsAT NP_001350692.1:n.-3-2937_-3-2936delinsAT
NM_000077.5:c.150+533_150+534delinsAT MANE Select NP_000068.1:n.150+533_150+534delinsAT
NM_001195132.2:c.150+533_150+534delinsAT NP_001182061.1:n.150+533_150+534delinsAT
NM_058195.4:c.194-2937_194-2936delinsAT MANE Plus Clinical NP_478102.2:n.194-2937_194-2936delinsAT
NM_058197.5:c.*73+259_*73+260delinsAT NP_478104.2:n.*73+259_*73+260delinsAT