Canonical Allele Identifier: CA645552473

Gene: CDKN2A

Linked Data

• COSMIC: COSM13700

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21971095_21971115del , CM000671.2:g.21971095_21971115del	GRCh38
NC_000009.11:g.21971094_21971114del , CM000671.1:g.21971094_21971114del	GRCh37
NC_000009.10:g.21961094_21961114del	NCBI36
NG_007485.1:g.28378_28398del , LRG_11:g.28378_28398del

Transcript Alleles

HGVS	Amino-acid change
ENST00000304494.10:c.245_265del MANE Select	ENSP00000307101.5:p.Val82_Glu88del
ENST00000404796.3:c.348-58338_348-58318del	ENSP00000385916.2:n.348-58338_348-58318de...
ENST00000579755.2:c.288_308del MANE Plus Clinical	ENSP00000462950.1:p.Ala97_Gly103del
ENST00000304494.9:c.245_265del	ENSP00000307101.5:p.Val82_Glu88del
ENST00000361570.4:c.287_307del	ENSP00000355153.4:p.Val96_Glu102del
ENST00000380150.2:n.219_239del
ENST00000380151.3:c.519_539del	ENSP00000369496.3:n.519_539del
ENST00000404796.2:c.348-58338_348-58318del	ENSP00000385916.2:n.348-58338_348-58318de...
ENST00000479692.2:c.92_112del	ENSP00000466887.1:p.Val31_Glu37del
ENST00000494262.5:c.92_112del	ENSP00000464952.1:p.Val31_Glu37del
ENST00000497750.1:c.92_112del	ENSP00000468510.1:p.Val31_Glu37del
ENST00000498124.1:c.245_265del	ENSP00000418915.1:p.Val82_Glu88del
ENST00000498628.6:c.92_112del	ENSP00000467857.1:p.Val31_Glu37del
ENST00000530628.2:c.288_308del	ENSP00000432664.2:p.Ala97_Gly103del
ENST00000578845.2:c.92_112del	ENSP00000467390.1:p.Val31_Glu37del
ENST00000579122.1:c.245_265del	ENSP00000464202.1:p.Val82_Glu88del
ENST00000579755.1:c.288_308del	ENSP00000462950.1:p.Ala97_Gly103del
NM_000077.4:c.245_265del , LRG_11t1:c.245_265del	NP_000068.1:p.Val82_Glu88del
NM_001195132.1:c.245_265del	NP_001182061.1:p.Val82_Glu88del
NM_058195.3:c.288_308del , LRG_11t2:c.288_308del	NP_478102.2:p.Ala97_Gly103del
NM_058197.4:c.519_539del	NP_478104.2:n.519_539del
XM_005251343.1:c.92_112del	XP_005251400.1:p.Val31_Glu37del
XM_011517675.1:c.245_265del	XP_011515977.1:p.Val82_Glu88del
XM_011517676.1:c.245_265del	XP_011515978.1:p.Val82_Glu88del
XM_011517679.1:c.92_112del	XP_011515981.1:p.Val31_Glu37del
XR_929159.1:n.646_666del
XR_929161.1:n.435_455del
XR_929162.1:n.435_455del
XR_929163.1:n.384_404del
XR_929164.1:n.167_187del
NM_001363763.1:c.92_112del	NP_001350692.1:p.Val31_Glu37del
XM_011517675.2:c.245_265del	XP_011515977.1:p.Val82_Glu88del
XM_011517676.2:c.245_265del	XP_011515978.1:p.Val82_Glu88del
XR_929159.2:n.575_595del
NM_001363763.2:c.92_112del	NP_001350692.1:p.Val31_Glu37del
NM_000077.5:c.245_265del MANE Select	NP_000068.1:p.Val82_Glu88del
NM_001195132.2:c.245_265del	NP_001182061.1:p.Val82_Glu88del
NM_058195.4:c.288_308del MANE Plus Clinical	NP_478102.2:p.Ala97_Gly103del
NM_058197.5:c.*168_*188del	NP_478104.2:n.*168_*188del