Canonical Allele Identifier: CA12951935
Gene: CDKN2A HGNC NCBI

Linked Data

dbSNP Id: rs3731239

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.21974219A>G , CM000671.2:g.21974219A>G GRCh38
NC_000009.11:g.21974218A>G , CM000671.1:g.21974218A>G GRCh37
NC_000009.10:g.21964218A>G NCBI36
NG_007485.1:g.25273T>C , LRG_11:g.25273T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000304494.10:c.150+459T>C MANE Select ENSP00000307101.5:p.=
ENST00000404796.3:c.348-55214A>G ENSP00000385916.2:p.=
ENST00000579755.2:c.194-3011T>C MANE Plus Clinical ENSP00000462950.1:p.=
ENST00000304494.9:c.150+459T>C ENSP00000307101.5:p.=
ENST00000361570.4:c.194-3011T>C ENSP00000355153.4:p.=
ENST00000380151.3:n.424+185T>C ENSP00000369496.3:p.=
ENST00000404796.2:c.348-55214A>G ENSP00000385916.2:p.=
ENST00000494262.5:c.-3-3011T>C ENSP00000464952.1:p.=
ENST00000498124.1:c.150+459T>C ENSP00000418915.1:p.=
ENST00000498628.6:c.-3-3011T>C ENSP00000467857.1:p.=
ENST00000530628.2:c.194-3011T>C ENSP00000432664.2:p.=
ENST00000579122.1:c.150+459T>C ENSP00000464202.1:p.=
ENST00000579755.1:c.194-3011T>C ENSP00000462950.1:p.=
NM_000077.4:c.150+459T>C , LRG_11t1:c.150+459T>C NP_000068.1:p.=
NM_001195132.1:c.150+459T>C NP_001182061.1:p.=
NM_058195.3:c.194-3011T>C , LRG_11t2:c.194-3011T>C NP_478102.2:p.=
NM_058197.4:n.424+185T>C NP_478104.2:p.=
XM_011517675.1:c.150+459T>C XP_011515977.1:p.=
XM_011517676.1:c.150+459T>C XP_011515978.1:p.=
XM_011517679.1:c.-3-3011T>C XP_011515981.1:p.=
XR_929159.1:n.551+459T>C
XR_929161.1:n.341-3011T>C
XR_929162.1:n.341-3011T>C
XR_929163.1:n.290-3011T>C
NM_001363763.1:c.-3-3011T>C NP_001350692.1:p.=
XM_011517675.2:c.150+459T>C XP_011515977.1:p.=
XM_011517676.2:c.150+459T>C XP_011515978.1:p.=
XR_929159.2:n.480+459T>C
NM_001363763.2:c.-3-3011T>C NP_001350692.1:p.=
NM_000077.5:c.150+459T>C MANE Select NP_000068.1:p.=
NM_001195132.2:c.150+459T>C NP_001182061.1:p.=
NM_058195.4:c.194-3011T>C MANE Plus Clinical NP_478102.2:p.=
NM_058197.5:c.*73+185T>C NP_478104.2:p.=