Canonical Allele Identifier: CA464261915

Gene: CDKN2A

Linked Data

• COSMIC: COSM13810
• MyVariant Identifiers: chr9:g.21971092del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21971095del , CM000671.2:g.21971095del	GRCh38
NC_000009.11:g.21971094del , CM000671.1:g.21971094del	GRCh37
NC_000009.10:g.21961094del	NCBI36
NG_007485.1:g.28399del , LRG_11:g.28399del

Transcript Alleles

HGVS	Amino-acid change
ENST00000304494.10:c.266del MANE Select	ENSP00000307101.5:p.Gly89AlafsTer?
ENST00000404796.3:c.348-58338del	ENSP00000385916.2:n.348-58338del
ENST00000579755.2:c.309del MANE Plus Clinical	ENSP00000462950.1:p.Leu104PhefsTer?
ENST00000304494.9:c.266del	ENSP00000307101.5:p.Gly89AlafsTer?
ENST00000361570.4:c.308del	ENSP00000355153.4:p.Gly103AlafsTer?
ENST00000380150.2:n.240del
ENST00000380151.3:c.540del	ENSP00000369496.3:n.540del
ENST00000404796.2:c.348-58338del	ENSP00000385916.2:n.348-58338del
ENST00000479692.2:c.113del	ENSP00000466887.1:p.Gly38AlafsTer?
ENST00000494262.5:c.113del	ENSP00000464952.1:p.Gly38AlafsTer?
ENST00000497750.1:c.113del	ENSP00000468510.1:p.Gly38AlafsTer?
ENST00000498124.1:c.266del	ENSP00000418915.1:p.Gly89AlafsTer?
ENST00000498628.6:c.113del	ENSP00000467857.1:p.Gly38AlafsTer?
ENST00000530628.2:c.309del	ENSP00000432664.2:p.Leu104PhefsTer?
ENST00000578845.2:c.113del	ENSP00000467390.1:p.Gly38AlafsTer?
ENST00000579122.1:c.266del	ENSP00000464202.1:p.Gly89AlafsTer?
ENST00000579755.1:c.309del	ENSP00000462950.1:p.Leu104PhefsTer?
NM_000077.4:c.266del , LRG_11t1:c.266del	NP_000068.1:p.Gly89AlafsTer?
NM_001195132.1:c.266del	NP_001182061.1:p.Gly89AlafsTer?
NM_058195.3:c.309del , LRG_11t2:c.309del	NP_478102.2:p.Leu104PhefsTer?
NM_058197.4:c.540del	NP_478104.2:n.540del
XM_005251343.1:c.113del	XP_005251400.1:p.Gly38AlafsTer?
XM_011517675.1:c.266del	XP_011515977.1:p.Gly89AlafsTer?
XM_011517676.1:c.266del	XP_011515978.1:p.Gly89AlafsTer?
XM_011517679.1:c.113del	XP_011515981.1:p.Gly38AlafsTer?
XR_929159.1:n.667del
XR_929161.1:n.456del
XR_929162.1:n.456del
XR_929163.1:n.405del
XR_929164.1:n.188del
NM_001363763.1:c.113del	NP_001350692.1:p.Gly38AlafsTer?
XM_011517675.2:c.266del	XP_011515977.1:p.Gly89AlafsTer?
XM_011517676.2:c.266del	XP_011515978.1:p.Gly89AlafsTer?
XR_929159.2:n.596del
NM_001363763.2:c.113del	NP_001350692.1:p.Gly38AlafsTer?
NM_000077.5:c.266del MANE Select	NP_000068.1:p.Gly89AlafsTer?
NM_001195132.2:c.266del	NP_001182061.1:p.Gly89AlafsTer?
NM_058195.4:c.309del MANE Plus Clinical	NP_478102.2:p.Leu104PhefsTer?
NM_058197.5:c.*189del	NP_478104.2:n.*189del