Canonical Allele Identifier: CA464261804
Gene: CDKN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1737984
dbSNP Id: rs1819685049
gnomAD v3: 9-21970948-G-A
gnomAD v4: 9-21970948-G-A
MyVariant Identifiers: chr9:g.21970947G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.21970948G>A , CM000671.2:g.21970948G>A GRCh38
NC_000009.11:g.21970947G>A , CM000671.1:g.21970947G>A GRCh37
NC_000009.10:g.21960947G>A NCBI36
NG_007485.1:g.28544C>T , LRG_11:g.28544C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000304494.10:c.411C>T MANE Select ENSP00000307101.5:p.Thr137=
ENST00000404796.3:c.348-58485G>A ENSP00000385916.2:n.348-58485G>A
ENST00000579755.2:c.*55C>T MANE Plus Clinical ENSP00000462950.1:n.*55C>T
ENST00000304494.9:c.411C>T ENSP00000307101.5:p.Thr137=
ENST00000361570.4:c.453C>T ENSP00000355153.4:p.Thr151=
ENST00000380150.2:n.385C>T
ENST00000380151.3:c.685C>T ENSP00000369496.3:n.685C>T
ENST00000404796.2:c.348-58485G>A ENSP00000385916.2:n.348-58485G>A
ENST00000479692.2:c.258C>T ENSP00000466887.1:p.Thr86=
ENST00000494262.5:c.258C>T ENSP00000464952.1:p.Thr86=
ENST00000497750.1:c.258C>T ENSP00000468510.1:p.Thr86=
ENST00000498124.1:c.411C>T ENSP00000418915.1:p.Thr137=
ENST00000498628.6:c.258C>T ENSP00000467857.1:p.Thr86=
ENST00000530628.2:c.*27+28C>T ENSP00000432664.2:n.*27+28C>T
ENST00000578845.2:c.258C>T ENSP00000467390.1:p.Thr86=
ENST00000579122.1:c.383+28C>T ENSP00000464202.1:n.383+28C>T
ENST00000579755.1:c.*55C>T ENSP00000462950.1:n.*55C>T
NM_000077.4:c.411C>T , LRG_11t1:c.411C>T NP_000068.1:p.Thr137=
NM_001195132.1:c.411C>T NP_001182061.1:p.Thr137=
NM_058195.3:c.*55C>T , LRG_11t2:c.*55C>T NP_478102.2:n.*55C>T
NM_058197.4:c.685C>T NP_478104.2:n.685C>T
XM_005251343.1:c.258C>T XP_005251400.1:p.Thr86=
XM_011517675.1:c.411C>T XP_011515977.1:p.Thr137=
XM_011517676.1:c.411C>T XP_011515978.1:p.Thr137=
XM_011517679.1:c.258C>T XP_011515981.1:p.Thr86=
XR_929159.1:n.812C>T
XR_929161.1:n.601C>T
XR_929162.1:n.601C>T
XR_929163.1:n.550C>T
XR_929164.1:n.333C>T
NM_001363763.1:c.258C>T NP_001350692.1:p.Thr86=
XM_011517675.2:c.411C>T XP_011515977.1:p.Thr137=
XM_011517676.2:c.411C>T XP_011515978.1:p.Thr137=
XR_929159.2:n.741C>T
NM_001363763.2:c.258C>T NP_001350692.1:p.Thr86=
NM_000077.5:c.411C>T MANE Select NP_000068.1:p.Thr137=
NM_001195132.2:c.411C>T NP_001182061.1:p.Thr137=
NM_058195.4:c.*55C>T MANE Plus Clinical NP_478102.2:n.*55C>T
NM_058197.5:c.*334C>T NP_478104.2:n.*334C>T