Canonical Allele Identifier: CA2718872792

Gene: CDKN2A

Linked Data

• dbSNP Id: rs1445495468

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21970839A>G , CM000671.2:g.21970839A>G	GRCh38
NC_000009.11:g.21970838A>G , CM000671.1:g.21970838A>G	GRCh37
NC_000009.10:g.21960838A>G	NCBI36
NG_007485.1:g.28653T>C , LRG_11:g.28653T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000304494.10:c.457+63T>C MANE Select	ENSP00000307101.5:n.457+63T>C
ENST00000404796.3:c.348-58594A>G	ENSP00000385916.2:n.348-58594A>G
ENST00000579755.2:c.*101+63T>C MANE Plus Clinical	ENSP00000462950.1:n.*101+63T>C
ENST00000304494.9:c.457+63T>C	ENSP00000307101.5:n.457+63T>C
ENST00000361570.4:c.499+63T>C	ENSP00000355153.4:n.499+63T>C
ENST00000380150.2:n.431+63T>C
ENST00000380151.3:c.731+63T>C	ENSP00000369496.3:n.731+63T>C
ENST00000404796.2:c.348-58594A>G	ENSP00000385916.2:n.348-58594A>G
ENST00000479692.2:c.304+63T>C	ENSP00000466887.1:n.304+63T>C
ENST00000494262.5:c.304+63T>C	ENSP00000464952.1:n.304+63T>C
ENST00000497750.1:c.*52T>C	ENSP00000468510.1:n.*52T>C
ENST00000498124.1:c.457+63T>C	ENSP00000418915.1:n.457+63T>C
ENST00000498628.6:c.304+63T>C	ENSP00000467857.1:n.304+63T>C
ENST00000530628.2:c.*27+137T>C	ENSP00000432664.2:n.*27+137T>C
ENST00000578845.2:c.304+63T>C	ENSP00000467390.1:n.304+63T>C
ENST00000579122.1:c.383+137T>C	ENSP00000464202.1:n.383+137T>C
ENST00000579755.1:c.*101+63T>C	ENSP00000462950.1:n.*101+63T>C
NM_000077.4:c.457+63T>C , LRG_11t1:c.457+63T>C	NP_000068.1:n.457+63T>C
NM_001195132.1:c.457+63T>C	NP_001182061.1:n.457+63T>C
NM_058195.3:c.*101+63T>C , LRG_11t2:c.*101+63T>C	NP_478102.2:n.*101+63T>C
NM_058197.4:c.731+63T>C	NP_478104.2:n.731+63T>C
XM_005251343.1:c.304+63T>C	XP_005251400.1:n.304+63T>C
XM_011517675.1:c.457+63T>C	XP_011515977.1:n.457+63T>C
XM_011517676.1:c.457+63T>C	XP_011515978.1:n.457+63T>C
XM_011517679.1:c.304+63T>C	XP_011515981.1:n.304+63T>C
XR_929159.1:n.858+63T>C
XR_929161.1:n.647+63T>C
XR_929162.1:n.647+63T>C
XR_929163.1:n.596+63T>C
XR_929164.1:n.379+63T>C
NM_001363763.1:c.304+63T>C	NP_001350692.1:n.304+63T>C
XM_011517675.2:c.457+63T>C	XP_011515977.1:n.457+63T>C
XM_011517676.2:c.457+63T>C	XP_011515978.1:n.457+63T>C
XR_929159.2:n.787+63T>C
NM_001363763.2:c.304+63T>C	NP_001350692.1:n.304+63T>C
NM_000077.5:c.457+63T>C MANE Select	NP_000068.1:n.457+63T>C
NM_001195132.2:c.457+63T>C	NP_001182061.1:n.457+63T>C
NM_058195.4:c.*101+63T>C MANE Plus Clinical	NP_478102.2:n.*101+63T>C
NM_058197.5:c.*380+63T>C	NP_478104.2:n.*380+63T>C