Canonical Allele Identifier: CA5012171

Gene: CDKN2A

Linked Data

• ClinVar Variation Id: 582036
• ClinVar RCV Id: RCV000706009 ; RCV000771468
• dbSNP Id: rs34170727
• ExAC: 9:21970988 G / C
• gnomAD v2: 9-21970988-G-C
• gnomAD v3: 9-21970989-G-C
• gnomAD v4: 9-21970989-G-C
• MyVariant Identifiers: chr9:g.21970988G>C (hg19) ; chr9:g.21970989G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21970989G>C , CM000671.2:g.21970989G>C	GRCh38
NC_000009.11:g.21970988G>C , CM000671.1:g.21970988G>C	GRCh37
NC_000009.10:g.21960988G>C	NCBI36
NG_007485.1:g.28503C>G , LRG_11:g.28503C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000304494.10:c.370C>G MANE Select	ENSP00000307101.5:p.Arg124Gly
ENST00000404796.3:c.348-58444G>C	ENSP00000385916.2:n.348-58444G>C
ENST00000579755.2:c.*14C>G MANE Plus Clinical	ENSP00000462950.1:n.*14C>G
ENST00000304494.9:c.370C>G	ENSP00000307101.5:p.Arg124Gly
ENST00000361570.4:c.412C>G	ENSP00000355153.4:p.Arg138Gly
ENST00000380150.2:n.344C>G
ENST00000380151.3:c.644C>G	ENSP00000369496.3:n.644C>G
ENST00000404796.2:c.348-58444G>C	ENSP00000385916.2:n.348-58444G>C
ENST00000479692.2:c.217C>G	ENSP00000466887.1:p.Arg73Gly
ENST00000494262.5:c.217C>G	ENSP00000464952.1:p.Arg73Gly
ENST00000497750.1:c.217C>G	ENSP00000468510.1:p.Arg73Gly
ENST00000498124.1:c.370C>G	ENSP00000418915.1:p.Arg124Gly
ENST00000498628.6:c.217C>G	ENSP00000467857.1:p.Arg73Gly
ENST00000530628.2:c.*14C>G	ENSP00000432664.2:n.*14C>G
ENST00000578845.2:c.217C>G	ENSP00000467390.1:p.Arg73Gly
ENST00000579122.1:c.370C>G	ENSP00000464202.1:p.Arg124Gly
ENST00000579755.1:c.*14C>G	ENSP00000462950.1:n.*14C>G
NM_000077.4:c.370C>G , LRG_11t1:c.370C>G	NP_000068.1:p.Arg124Gly
NM_001195132.1:c.370C>G	NP_001182061.1:p.Arg124Gly
NM_058195.3:c.*14C>G , LRG_11t2:c.*14C>G	NP_478102.2:n.*14C>G
NM_058197.4:c.644C>G	NP_478104.2:n.644C>G
XM_005251343.1:c.217C>G	XP_005251400.1:p.Arg73Gly
XM_011517675.1:c.370C>G	XP_011515977.1:p.Arg124Gly
XM_011517676.1:c.370C>G	XP_011515978.1:p.Arg124Gly
XM_011517679.1:c.217C>G	XP_011515981.1:p.Arg73Gly
XR_929159.1:n.771C>G
XR_929161.1:n.560C>G
XR_929162.1:n.560C>G
XR_929163.1:n.509C>G
XR_929164.1:n.292C>G
NM_001363763.1:c.217C>G	NP_001350692.1:p.Arg73Gly
XM_011517675.2:c.370C>G	XP_011515977.1:p.Arg124Gly
XM_011517676.2:c.370C>G	XP_011515978.1:p.Arg124Gly
XR_929159.2:n.700C>G
NM_001363763.2:c.217C>G	NP_001350692.1:p.Arg73Gly
NM_000077.5:c.370C>G MANE Select	NP_000068.1:p.Arg124Gly
NM_001195132.2:c.370C>G	NP_001182061.1:p.Arg124Gly
NM_058195.4:c.*14C>G MANE Plus Clinical	NP_478102.2:n.*14C>G
NM_058197.5:c.*293C>G	NP_478104.2:n.*293C>G