Canonical Allele Identifier: CA645552436
Gene: CDKN2A HGNC NCBI

Linked Data

COSMIC: COSM12545

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.21971002_21971006delinsT , CM000671.2:g.21971002_21971006delinsT GRCh38
NC_000009.11:g.21971001_21971005delinsT , CM000671.1:g.21971001_21971005delinsT GRCh37
NC_000009.10:g.21961001_21961005delinsT NCBI36
NG_007485.1:g.28486_28490delinsA , LRG_11:g.28486_28490delinsA

Transcript Alleles

HGVS Amino-acid change
ENST00000304494.10:c.353_357delinsA MANE Select ENSP00000307101.5:p.Ala118GlufsTer27
ENST00000404796.3:c.348-58431_348-58427delinsT ENSP00000385916.2:n.348-58431_348-58427de...
ENST00000579755.2:c.396_*1delinsA MANE Plus Clinical ENSP00000462950.1:n.[c.396_*1delinsA;Ter1...
ENST00000304494.9:c.353_357delinsA ENSP00000307101.5:p.Ala118GlufsTer27
ENST00000361570.4:c.395_399delinsA ENSP00000355153.4:p.Ala132GlufsTer27
ENST00000380150.2:n.327_331delinsA
ENST00000380151.3:c.627_631delinsA ENSP00000369496.3:n.627_631delinsA
ENST00000404796.2:c.348-58431_348-58427delinsT ENSP00000385916.2:n.348-58431_348-58427de...
ENST00000479692.2:c.200_204delinsA ENSP00000466887.1:p.Ala67GlufsTer27
ENST00000494262.5:c.200_204delinsA ENSP00000464952.1:p.Ala67GlufsTer27
ENST00000497750.1:c.200_204delinsA ENSP00000468510.1:p.Ala67GlufsTer27
ENST00000498124.1:c.353_357delinsA ENSP00000418915.1:p.Ala118GlufsTer27
ENST00000498628.6:c.200_204delinsA ENSP00000467857.1:p.Ala67GlufsTer27
ENST00000530628.2:c.396_*1delinsA ENSP00000432664.2:n.[c.396_*1delinsA;Ter1...
ENST00000578845.2:c.200_204delinsA ENSP00000467390.1:p.Ala67GlufsTer27
ENST00000579122.1:c.353_357delinsA ENSP00000464202.1:p.Ala118GlufsTer14
ENST00000579755.1:c.396_*1delinsA ENSP00000462950.1:n.[c.396_*1delinsA;Ter1...
NM_000077.4:c.353_357delinsA , LRG_11t1:c.353_357delinsA NP_000068.1:p.Ala118GlufsTer27
NM_001195132.1:c.353_357delinsA NP_001182061.1:p.Ala118GlufsTer27
NM_058195.3:c.396_*1delinsA , LRG_11t2:c.396_*1delinsA NP_478102.2:n.[c.396_*1delinsA;Ter133Glue...
NM_058197.4:c.627_631delinsA NP_478104.2:n.627_631delinsA
XM_005251343.1:c.200_204delinsA XP_005251400.1:p.Ala67GlufsTer27
XM_011517675.1:c.353_357delinsA XP_011515977.1:p.Ala118GlufsTer27
XM_011517676.1:c.353_357delinsA XP_011515978.1:p.Ala118GlufsTer27
XM_011517679.1:c.200_204delinsA XP_011515981.1:p.Ala67GlufsTer27
XR_929159.1:n.754_758delinsA
XR_929161.1:n.543_547delinsA
XR_929162.1:n.543_547delinsA
XR_929163.1:n.492_496delinsA
XR_929164.1:n.275_279delinsA
NM_001363763.1:c.200_204delinsA NP_001350692.1:p.Ala67GlufsTer27
XM_011517675.2:c.353_357delinsA XP_011515977.1:p.Ala118GlufsTer27
XM_011517676.2:c.353_357delinsA XP_011515978.1:p.Ala118GlufsTer27
XR_929159.2:n.683_687delinsA
NM_001363763.2:c.200_204delinsA NP_001350692.1:p.Ala67GlufsTer27
NM_000077.5:c.353_357delinsA MANE Select NP_000068.1:p.Ala118GlufsTer27
NM_001195132.2:c.353_357delinsA NP_001182061.1:p.Ala118GlufsTer27
NM_058195.4:c.396_*1delinsA MANE Plus Clinical NP_478102.2:n.[c.396_*1delinsA;Ter133Glue...
NM_058197.5:c.*276_*280delinsA NP_478104.2:n.*276_*280delinsA