Canonical Allele Identifier: CA373085895
Gene: CDKN2A HGNC NCBI

Linked Data

gnomAD v4: 9-21970949-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.21970949G>T , CM000671.2:g.21970949G>T GRCh38
NC_000009.11:g.21970948G>T , CM000671.1:g.21970948G>T GRCh37
NC_000009.10:g.21960948G>T NCBI36
NG_007485.1:g.28543C>A , LRG_11:g.28543C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000304494.10:c.410C>A MANE Select ENSP00000307101.5:p.Thr137Asn
ENST00000404796.3:c.348-58484G>T ENSP00000385916.2:n.348-58484G>T
ENST00000579755.2:c.*54C>A MANE Plus Clinical ENSP00000462950.1:n.*54C>A
ENST00000304494.9:c.410C>A ENSP00000307101.5:p.Thr137Asn
ENST00000361570.4:c.452C>A ENSP00000355153.4:p.Thr151Asn
ENST00000380150.2:n.384C>A
ENST00000380151.3:c.684C>A ENSP00000369496.3:n.684C>A
ENST00000404796.2:c.348-58484G>T ENSP00000385916.2:n.348-58484G>T
ENST00000479692.2:c.257C>A ENSP00000466887.1:p.Thr86Asn
ENST00000494262.5:c.257C>A ENSP00000464952.1:p.Thr86Asn
ENST00000497750.1:c.257C>A ENSP00000468510.1:p.Thr86Asn
ENST00000498124.1:c.410C>A ENSP00000418915.1:p.Thr137Asn
ENST00000498628.6:c.257C>A ENSP00000467857.1:p.Thr86Asn
ENST00000530628.2:c.*27+27C>A ENSP00000432664.2:n.*27+27C>A
ENST00000578845.2:c.257C>A ENSP00000467390.1:p.Thr86Asn
ENST00000579122.1:c.383+27C>A ENSP00000464202.1:n.383+27C>A
ENST00000579755.1:c.*54C>A ENSP00000462950.1:n.*54C>A
NM_000077.4:c.410C>A , LRG_11t1:c.410C>A NP_000068.1:p.Thr137Asn
NM_001195132.1:c.410C>A NP_001182061.1:p.Thr137Asn
NM_058195.3:c.*54C>A , LRG_11t2:c.*54C>A NP_478102.2:n.*54C>A
NM_058197.4:c.684C>A NP_478104.2:n.684C>A
XM_005251343.1:c.257C>A XP_005251400.1:p.Thr86Asn
XM_011517675.1:c.410C>A XP_011515977.1:p.Thr137Asn
XM_011517676.1:c.410C>A XP_011515978.1:p.Thr137Asn
XM_011517679.1:c.257C>A XP_011515981.1:p.Thr86Asn
XR_929159.1:n.811C>A
XR_929161.1:n.600C>A
XR_929162.1:n.600C>A
XR_929163.1:n.549C>A
XR_929164.1:n.332C>A
NM_001363763.1:c.257C>A NP_001350692.1:p.Thr86Asn
XM_011517675.2:c.410C>A XP_011515977.1:p.Thr137Asn
XM_011517676.2:c.410C>A XP_011515978.1:p.Thr137Asn
XR_929159.2:n.740C>A
NM_001363763.2:c.257C>A NP_001350692.1:p.Thr86Asn
NM_000077.5:c.410C>A MANE Select NP_000068.1:p.Thr137Asn
NM_001195132.2:c.410C>A NP_001182061.1:p.Thr137Asn
NM_058195.4:c.*54C>A MANE Plus Clinical NP_478102.2:n.*54C>A
NM_058197.5:c.*333C>A NP_478104.2:n.*333C>A