Canonical Allele Identifier: CA645552564
Gene: CDKN2A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.21971187_21971188delinsAA , CM000671.2:g.21971187_21971188delinsAA GRCh38
NC_000009.11:g.21971186_21971187delinsAA , CM000671.1:g.21971186_21971187delinsAA GRCh37
NC_000009.10:g.21961186_21961187delinsAA NCBI36
NG_007485.1:g.28304_28305delinsTT , LRG_11:g.28304_28305delinsTT

Transcript Alleles

HGVS Amino-acid change
ENST00000304494.10:c.171_172delinsTT MANE Select ENSP00000307101.5:p.Ala58Ter
ENST00000404796.3:c.348-58246_348-58245delinsAA ENSP00000385916.2:n.348-58246_348-58245de...
ENST00000579755.2:c.214_215delinsTT MANE Plus Clinical ENSP00000462950.1:p.Pro72Leu
ENST00000304494.9:c.171_172delinsTT ENSP00000307101.5:p.Ala58Ter
ENST00000361570.4:c.214_215delinsTT ENSP00000355153.4:p.Pro72Leu
ENST00000380150.2:n.145_146delinsTT
ENST00000380151.3:c.445_446delinsTT ENSP00000369496.3:n.445_446delinsTT
ENST00000404796.2:c.348-58246_348-58245delinsAA ENSP00000385916.2:n.348-58246_348-58245de...
ENST00000479692.2:c.18_19delinsTT ENSP00000466887.1:p.Ala7Ter
ENST00000494262.5:c.18_19delinsTT ENSP00000464952.1:p.Ala7Ter
ENST00000497750.1:c.18_19delinsTT ENSP00000468510.1:p.Ala7Ter
ENST00000498124.1:c.171_172delinsTT ENSP00000418915.1:p.Ala58Ter
ENST00000498628.6:c.18_19delinsTT ENSP00000467857.1:p.Ala7Ter
ENST00000530628.2:c.214_215delinsTT ENSP00000432664.2:p.Pro72Leu
ENST00000578845.2:c.18_19delinsTT ENSP00000467390.1:p.Ala7Ter
ENST00000579122.1:c.171_172delinsTT ENSP00000464202.1:p.Ala58Ter
ENST00000579755.1:c.214_215delinsTT ENSP00000462950.1:p.Pro72Leu
NM_000077.4:c.171_172delinsTT , LRG_11t1:c.171_172delinsTT NP_000068.1:p.Ala58Ter
NM_001195132.1:c.171_172delinsTT NP_001182061.1:p.Ala58Ter
NM_058195.3:c.214_215delinsTT , LRG_11t2:c.214_215delinsTT NP_478102.2:p.Pro72Leu
NM_058197.4:c.445_446delinsTT NP_478104.2:n.445_446delinsTT
XM_005251343.1:c.18_19delinsTT XP_005251400.1:p.Ala7Ter
XM_011517675.1:c.171_172delinsTT XP_011515977.1:p.Ala58Ter
XM_011517676.1:c.171_172delinsTT XP_011515978.1:p.Ala58Ter
XM_011517679.1:c.18_19delinsTT XP_011515981.1:p.Ala7Ter
XR_929159.1:n.572_573delinsTT
XR_929161.1:n.361_362delinsTT
XR_929162.1:n.361_362delinsTT
XR_929163.1:n.310_311delinsTT
XR_929164.1:n.93_94delinsTT
NM_001363763.1:c.18_19delinsTT NP_001350692.1:p.Ala7Ter
XM_011517675.2:c.171_172delinsTT XP_011515977.1:p.Ala58Ter
XM_011517676.2:c.171_172delinsTT XP_011515978.1:p.Ala58Ter
XR_929159.2:n.501_502delinsTT
NM_001363763.2:c.18_19delinsTT NP_001350692.1:p.Ala7Ter
NM_000077.5:c.171_172delinsTT MANE Select NP_000068.1:p.Ala58Ter
NM_001195132.2:c.171_172delinsTT NP_001182061.1:p.Ala58Ter
NM_058195.4:c.214_215delinsTT MANE Plus Clinical NP_478102.2:p.Pro72Leu
NM_058197.5:c.*94_*95delinsTT NP_478104.2:n.*94_*95delinsTT