Canonical Allele Identifier: CA645552600
Gene: CDKN2A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.21974691_21974695dup , CM000671.2:g.21974691_21974695dup GRCh38
NC_000009.11:g.21974690_21974694dup , CM000671.1:g.21974690_21974694dup GRCh37
NC_000009.10:g.21964690_21964694dup NCBI36
NG_007485.1:g.24798_24802dup , LRG_11:g.24798_24802dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000304494.10:c.134_138dup MANE Select ENSP00000307101.5:p.Arg47ValfsTer8
ENST00000404796.3:c.348-54742_348-54738dup ENSP00000385916.2:n.348-54742_348-54738dup
ENST00000579755.2:c.194-3486_194-3482dup MANE Plus Clinical ENSP00000462950.1:n.194-3486_194-3482dup
ENST00000304494.9:c.134_138dup ENSP00000307101.5:p.Arg47ValfsTer8
ENST00000361570.4:c.194-3486_194-3482dup ENSP00000355153.4:n.194-3486_194-3482dup
ENST00000380151.3:c.134_138dup ENSP00000369496.3:p.Arg47ValfsTer?
ENST00000404796.2:c.348-54742_348-54738dup ENSP00000385916.2:n.348-54742_348-54738dup
ENST00000494262.5:c.-3-3486_-3-3482dup ENSP00000464952.1:n.-3-3486_-3-3482dup
ENST00000498124.1:c.134_138dup ENSP00000418915.1:p.Arg47ValfsTer8
ENST00000498628.6:c.-3-3486_-3-3482dup ENSP00000467857.1:n.-3-3486_-3-3482dup
ENST00000530628.2:c.194-3486_194-3482dup ENSP00000432664.2:n.194-3486_194-3482dup
ENST00000579122.1:c.134_138dup ENSP00000464202.1:p.Arg47ValfsTer8
ENST00000579755.1:c.194-3486_194-3482dup ENSP00000462950.1:n.194-3486_194-3482dup
NM_000077.4:c.134_138dup , LRG_11t1:c.134_138dup NP_000068.1:p.Arg47ValfsTer8
NM_001195132.1:c.134_138dup NP_001182061.1:p.Arg47ValfsTer8
NM_058195.3:c.194-3486_194-3482dup , LRG_11t2:c.194-3486_194-3482dup NP_478102.2:n.194-3486_194-3482dup
NM_058197.4:c.134_138dup NP_478104.2:p.Arg47ValfsTer?
XM_011517675.1:c.134_138dup XP_011515977.1:p.Arg47ValfsTer8
XM_011517676.1:c.134_138dup XP_011515978.1:p.Arg47ValfsTer8
XM_011517679.1:c.-3-3486_-3-3482dup XP_011515981.1:n.-3-3486_-3-3482dup
XR_929159.1:n.535_539dup
XR_929161.1:n.341-3486_341-3482dup
XR_929162.1:n.341-3486_341-3482dup
XR_929163.1:n.290-3486_290-3482dup
NM_001363763.1:c.-3-3486_-3-3482dup NP_001350692.1:n.-3-3486_-3-3482dup
XM_011517675.2:c.134_138dup XP_011515977.1:p.Arg47ValfsTer8
XM_011517676.2:c.134_138dup XP_011515978.1:p.Arg47ValfsTer8
XR_929159.2:n.464_468dup
NM_001363763.2:c.-3-3486_-3-3482dup NP_001350692.1:n.-3-3486_-3-3482dup
NM_000077.5:c.134_138dup MANE Select NP_000068.1:p.Arg47ValfsTer8
NM_001195132.2:c.134_138dup NP_001182061.1:p.Arg47ValfsTer8
NM_058195.4:c.194-3486_194-3482dup MANE Plus Clinical NP_478102.2:n.194-3486_194-3482dup
NM_058197.5:c.134_138dup NP_478104.2:p.Arg47ValfsTer?