Canonical Allele Identifier: CA1839173429
Gene: CDKN2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.21974795A= , CM000671.2:g.21974795A= GRCh38
NC_000009.11:g.21974794A= , CM000671.1:g.21974794A= GRCh37
NC_000009.10:g.21964794A= NCBI36
NG_007485.1:g.24697T= , LRG_11:g.24697T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000304494.10:c.33T= MANE Select ENSP00000307101.5:p.Pro11=
ENST00000404796.3:c.348-54638A= ENSP00000385916.2:n.348-54638A=
ENST00000579755.2:c.194-3587T= MANE Plus Clinical ENSP00000462950.1:n.194-3587T=
ENST00000304494.9:c.33T= ENSP00000307101.5:p.Pro11=
ENST00000361570.4:c.194-3587T= ENSP00000355153.4:n.194-3587T=
ENST00000380151.3:c.33T= ENSP00000369496.3:p.Pro11=
ENST00000404796.2:c.348-54638A= ENSP00000385916.2:n.348-54638A=
ENST00000494262.5:c.-3-3587T= ENSP00000464952.1:n.-3-3587T=
ENST00000498124.1:c.33T= ENSP00000418915.1:p.Pro11=
ENST00000498628.6:c.-3-3587T= ENSP00000467857.1:n.-3-3587T=
ENST00000530628.2:c.194-3587T= ENSP00000432664.2:n.194-3587T=
ENST00000579122.1:c.33T= ENSP00000464202.1:p.Pro11=
ENST00000579755.1:c.194-3587T= ENSP00000462950.1:n.194-3587T=
NM_000077.4:c.33T= , LRG_11t1:c.33T= NP_000068.1:p.Pro11=
NM_001195132.1:c.33T= NP_001182061.1:p.Pro11=
NM_058195.3:c.194-3587T= , LRG_11t2:c.194-3587T= NP_478102.2:n.194-3587T=
NM_058197.4:c.33T= NP_478104.2:p.Pro11=
XM_011517675.1:c.33T= XP_011515977.1:p.Pro11=
XM_011517676.1:c.33T= XP_011515978.1:p.Pro11=
XM_011517679.1:c.-3-3587T= XP_011515981.1:n.-3-3587T=
XR_929159.1:n.434T=
XR_929161.1:n.341-3587T=
XR_929162.1:n.341-3587T=
XR_929163.1:n.290-3587T=
NM_001363763.1:c.-3-3587T= NP_001350692.1:n.-3-3587T=
XM_011517675.2:c.33T= XP_011515977.1:p.Pro11=
XM_011517676.2:c.33T= XP_011515978.1:p.Pro11=
XR_929159.2:n.363T=
NM_001363763.2:c.-3-3587T= NP_001350692.1:n.-3-3587T=
NM_000077.5:c.33T= MANE Select NP_000068.1:p.Pro11=
NM_001195132.2:c.33T= NP_001182061.1:p.Pro11=
NM_058195.4:c.194-3587T= MANE Plus Clinical NP_478102.2:n.194-3587T=
NM_058197.5:c.33T= NP_478104.2:p.Pro11=