Canonical Allele Identifier: CA645552472
Gene: CDKN2A HGNC NCBI

Linked Data

COSMIC: COSM13220

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.21971094_21971095delinsTT , CM000671.2:g.21971094_21971095delinsTT GRCh38
NC_000009.11:g.21971093_21971094delinsTT , CM000671.1:g.21971093_21971094delinsTT GRCh37
NC_000009.10:g.21961093_21961094delinsTT NCBI36
NG_007485.1:g.28397_28398delinsAA , LRG_11:g.28397_28398delinsAA

Transcript Alleles

HGVS Amino-acid change
ENST00000304494.10:c.264_265delinsAA MANE Select ENSP00000307101.5:p.Gly89Ser
ENST00000404796.3:c.348-58339_348-58338delinsTT ENSP00000385916.2:n.348-58339_348-58338de...
ENST00000579755.2:c.307_308delinsAA MANE Plus Clinical ENSP00000462950.1:p.Gly103Lys
ENST00000304494.9:c.264_265delinsAA ENSP00000307101.5:p.Gly89Ser
ENST00000361570.4:c.306_307delinsAA ENSP00000355153.4:p.Gly103Ser
ENST00000380150.2:n.238_239delinsAA
ENST00000380151.3:c.538_539delinsAA ENSP00000369496.3:n.538_539delinsAA
ENST00000404796.2:c.348-58339_348-58338delinsTT ENSP00000385916.2:n.348-58339_348-58338de...
ENST00000479692.2:c.111_112delinsAA ENSP00000466887.1:p.Gly38Ser
ENST00000494262.5:c.111_112delinsAA ENSP00000464952.1:p.Gly38Ser
ENST00000497750.1:c.111_112delinsAA ENSP00000468510.1:p.Gly38Ser
ENST00000498124.1:c.264_265delinsAA ENSP00000418915.1:p.Gly89Ser
ENST00000498628.6:c.111_112delinsAA ENSP00000467857.1:p.Gly38Ser
ENST00000530628.2:c.307_308delinsAA ENSP00000432664.2:p.Gly103Lys
ENST00000578845.2:c.111_112delinsAA ENSP00000467390.1:p.Gly38Ser
ENST00000579122.1:c.264_265delinsAA ENSP00000464202.1:p.Gly89Ser
ENST00000579755.1:c.307_308delinsAA ENSP00000462950.1:p.Gly103Lys
NM_000077.4:c.264_265delinsAA , LRG_11t1:c.264_265delinsAA NP_000068.1:p.Gly89Ser
NM_001195132.1:c.264_265delinsAA NP_001182061.1:p.Gly89Ser
NM_058195.3:c.307_308delinsAA , LRG_11t2:c.307_308delinsAA NP_478102.2:p.Gly103Lys
NM_058197.4:c.538_539delinsAA NP_478104.2:n.538_539delinsAA
XM_005251343.1:c.111_112delinsAA XP_005251400.1:p.Gly38Ser
XM_011517675.1:c.264_265delinsAA XP_011515977.1:p.Gly89Ser
XM_011517676.1:c.264_265delinsAA XP_011515978.1:p.Gly89Ser
XM_011517679.1:c.111_112delinsAA XP_011515981.1:p.Gly38Ser
XR_929159.1:n.665_666delinsAA
XR_929161.1:n.454_455delinsAA
XR_929162.1:n.454_455delinsAA
XR_929163.1:n.403_404delinsAA
XR_929164.1:n.186_187delinsAA
NM_001363763.1:c.111_112delinsAA NP_001350692.1:p.Gly38Ser
XM_011517675.2:c.264_265delinsAA XP_011515977.1:p.Gly89Ser
XM_011517676.2:c.264_265delinsAA XP_011515978.1:p.Gly89Ser
XR_929159.2:n.594_595delinsAA
NM_001363763.2:c.111_112delinsAA NP_001350692.1:p.Gly38Ser
NM_000077.5:c.264_265delinsAA MANE Select NP_000068.1:p.Gly89Ser
NM_001195132.2:c.264_265delinsAA NP_001182061.1:p.Gly89Ser
NM_058195.4:c.307_308delinsAA MANE Plus Clinical NP_478102.2:p.Gly103Lys
NM_058197.5:c.*187_*188delinsAA NP_478104.2:n.*187_*188delinsAA