Canonical Allele Identifier: CA373085080

Gene: CDKN2A

Linked Data

• dbSNP Id: rs778871932
• MyVariant Identifiers: chr9:g.21968240G>C (hg19) ; chr9:g.21968241G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21968241G>C , CM000671.2:g.21968241G>C	GRCh38
NC_000009.11:g.21968240G>C , CM000671.1:g.21968240G>C	GRCh37
NC_000009.10:g.21958240G>C	NCBI36
NG_007485.1:g.31251C>G , LRG_11:g.31251C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304494.10:c.459C>G MANE Select	ENSP00000307101.5:p.Asp153Glu
ENST00000404796.3:c.348-61192G>C	ENSP00000385916.2:n.348-61192G>C
ENST00000579755.2:c.*103C>G MANE Plus Clinical	ENSP00000462950.1:n.*103C>G
ENST00000304494.9:c.459C>G	ENSP00000307101.5:p.Asp153Glu
ENST00000361570.4:c.501C>G	ENSP00000355153.4:p.Asp167Glu
ENST00000380151.3:c.733C>G	ENSP00000369496.3:n.733C>G
ENST00000404796.2:c.348-61192G>C	ENSP00000385916.2:n.348-61192G>C
ENST00000494262.5:c.306C>G	ENSP00000464952.1:p.Asp102Glu
ENST00000498124.1:c.*152C>G	ENSP00000418915.1:n.*152C>G
ENST00000498628.6:c.306C>G	ENSP00000467857.1:p.Asp102Glu
ENST00000530628.2:c.*29C>G	ENSP00000432664.2:n.*29C>G
ENST00000578845.2:c.306C>G	ENSP00000467390.1:p.Asp102Glu
ENST00000579122.1:c.385C>G	ENSP00000464202.1:p.His129Asp
ENST00000579755.1:c.*103C>G	ENSP00000462950.1:n.*103C>G
NM_000077.4:c.459C>G , LRG_11t1:c.459C>G	NP_000068.1:p.Asp153Glu
NM_001195132.1:c.*152C>G	NP_001182061.1:n.*152C>G
NM_058195.3:c.*103C>G , LRG_11t2:c.*103C>G	NP_478102.2:n.*103C>G
NM_058197.4:c.733C>G	NP_478104.2:n.733C>G
XM_005251343.1:c.306C>G	XP_005251400.1:p.Asp102Glu
XM_011517679.1:c.306C>G	XP_011515981.1:p.Asp102Glu
NM_001363763.1:c.306C>G	NP_001350692.1:p.Asp102Glu
NM_001363763.2:c.306C>G	NP_001350692.1:p.Asp102Glu
NM_000077.5:c.459C>G MANE Select	NP_000068.1:p.Asp153Glu
NM_001195132.2:c.*152C>G	NP_001182061.1:n.*152C>G
NM_058195.4:c.*103C>G MANE Plus Clinical	NP_478102.2:n.*103C>G
NM_058197.5:c.*382C>G	NP_478104.2:n.*382C>G