Canonical Allele Identifier: CA2719026532

Gene: CDKN2A

Linked Data

• dbSNP Id: rs2131079382

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21968227T>C , CM000671.2:g.21968227T>C	GRCh38
NC_000009.11:g.21968226T>C , CM000671.1:g.21968226T>C	GRCh37
NC_000009.10:g.21958226T>C	NCBI36
NG_007485.1:g.31265A>G , LRG_11:g.31265A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304494.10:c.*2A>G MANE Select	ENSP00000307101.5:n.*2A>G
ENST00000404796.3:c.348-61206T>C	ENSP00000385916.2:n.348-61206T>C
ENST00000579755.2:c.*117A>G MANE Plus Clinical	ENSP00000462950.1:n.*117A>G
ENST00000304494.9:c.*2A>G	ENSP00000307101.5:n.*2A>G
ENST00000361570.4:c.*2A>G	ENSP00000355153.4:n.*2A>G
ENST00000380151.3:c.747A>G	ENSP00000369496.3:n.747A>G
ENST00000404796.2:c.348-61206T>C	ENSP00000385916.2:n.348-61206T>C
ENST00000494262.5:c.*2A>G	ENSP00000464952.1:n.*2A>G
ENST00000498124.1:c.*166A>G	ENSP00000418915.1:n.*166A>G
ENST00000498628.6:c.*2A>G	ENSP00000467857.1:n.*2A>G
ENST00000530628.2:c.*43A>G	ENSP00000432664.2:n.*43A>G
ENST00000578845.2:c.*2A>G	ENSP00000467390.1:n.*2A>G
ENST00000579122.1:c.399A>G	ENSP00000464202.1:p.Lys133=
ENST00000579755.1:c.*117A>G	ENSP00000462950.1:n.*117A>G
NM_000077.4:c.*2A>G , LRG_11t1:c.*2A>G	NP_000068.1:n.*2A>G
NM_001195132.1:c.*166A>G	NP_001182061.1:n.*166A>G
NM_058195.3:c.*117A>G , LRG_11t2:c.*117A>G	NP_478102.2:n.*117A>G
NM_058197.4:c.747A>G	NP_478104.2:n.747A>G
XM_005251343.1:c.*2A>G	XP_005251400.1:n.*2A>G
XM_011517679.1:c.*2A>G	XP_011515981.1:n.*2A>G
NM_001363763.1:c.*2A>G	NP_001350692.1:n.*2A>G
NM_001363763.2:c.*2A>G	NP_001350692.1:n.*2A>G
NM_000077.5:c.*2A>G MANE Select	NP_000068.1:n.*2A>G
NM_001195132.2:c.*166A>G	NP_001182061.1:n.*166A>G
NM_058195.4:c.*117A>G MANE Plus Clinical	NP_478102.2:n.*117A>G
NM_058197.5:c.*396A>G	NP_478104.2:n.*396A>G