Canonical Allele Identifier: CA373085964

Gene: CDKN2A

Linked Data

• ClinVar Variation Id: 824122
• ClinVar RCV Id: RCV001020969
• dbSNP Id: rs747621669
• MyVariant Identifiers: chr9:g.21970987C>G (hg19) ; chr9:g.21970988C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21970988C>G , CM000671.2:g.21970988C>G	GRCh38
NC_000009.11:g.21970987C>G , CM000671.1:g.21970987C>G	GRCh37
NC_000009.10:g.21960987C>G	NCBI36
NG_007485.1:g.28504G>C , LRG_11:g.28504G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000304494.10:c.371G>C MANE Select	ENSP00000307101.5:p.Arg124Pro
ENST00000404796.3:c.348-58445C>G	ENSP00000385916.2:n.348-58445C>G
ENST00000579755.2:c.*15G>C MANE Plus Clinical	ENSP00000462950.1:n.*15G>C
ENST00000304494.9:c.371G>C	ENSP00000307101.5:p.Arg124Pro
ENST00000361570.4:c.413G>C	ENSP00000355153.4:p.Arg138Pro
ENST00000380150.2:n.345G>C
ENST00000380151.3:c.645G>C	ENSP00000369496.3:n.645G>C
ENST00000404796.2:c.348-58445C>G	ENSP00000385916.2:n.348-58445C>G
ENST00000479692.2:c.218G>C	ENSP00000466887.1:p.Arg73Pro
ENST00000494262.5:c.218G>C	ENSP00000464952.1:p.Arg73Pro
ENST00000497750.1:c.218G>C	ENSP00000468510.1:p.Arg73Pro
ENST00000498124.1:c.371G>C	ENSP00000418915.1:p.Arg124Pro
ENST00000498628.6:c.218G>C	ENSP00000467857.1:p.Arg73Pro
ENST00000530628.2:c.*15G>C	ENSP00000432664.2:n.*15G>C
ENST00000578845.2:c.218G>C	ENSP00000467390.1:p.Arg73Pro
ENST00000579122.1:c.371G>C	ENSP00000464202.1:p.Arg124Pro
ENST00000579755.1:c.*15G>C	ENSP00000462950.1:n.*15G>C
NM_000077.4:c.371G>C , LRG_11t1:c.371G>C	NP_000068.1:p.Arg124Pro
NM_001195132.1:c.371G>C	NP_001182061.1:p.Arg124Pro
NM_058195.3:c.*15G>C , LRG_11t2:c.*15G>C	NP_478102.2:n.*15G>C
NM_058197.4:c.645G>C	NP_478104.2:n.645G>C
XM_005251343.1:c.218G>C	XP_005251400.1:p.Arg73Pro
XM_011517675.1:c.371G>C	XP_011515977.1:p.Arg124Pro
XM_011517676.1:c.371G>C	XP_011515978.1:p.Arg124Pro
XM_011517679.1:c.218G>C	XP_011515981.1:p.Arg73Pro
XR_929159.1:n.772G>C
XR_929161.1:n.561G>C
XR_929162.1:n.561G>C
XR_929163.1:n.510G>C
XR_929164.1:n.293G>C
NM_001363763.1:c.218G>C	NP_001350692.1:p.Arg73Pro
XM_011517675.2:c.371G>C	XP_011515977.1:p.Arg124Pro
XM_011517676.2:c.371G>C	XP_011515978.1:p.Arg124Pro
XR_929159.2:n.701G>C
NM_001363763.2:c.218G>C	NP_001350692.1:p.Arg73Pro
NM_000077.5:c.371G>C MANE Select	NP_000068.1:p.Arg124Pro
NM_001195132.2:c.371G>C	NP_001182061.1:p.Arg124Pro
NM_058195.4:c.*15G>C MANE Plus Clinical	NP_478102.2:n.*15G>C
NM_058197.5:c.*294G>C	NP_478104.2:n.*294G>C