Canonical Allele Identifier: CA645552604

Gene: CDKN2A

Linked Data

• COSMIC: COSM5760906 ; COSM5760907 ; COSM5760908

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21974706_21974707insAA , CM000671.2:g.21974706_21974707insAA	GRCh38
NC_000009.11:g.21974705_21974706insAA , CM000671.1:g.21974705_21974706insAA	GRCh37
NC_000009.10:g.21964705_21964706insAA	NCBI36
NG_007485.1:g.24785_24786insTT , LRG_11:g.24785_24786insTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304494.10:c.121_122insTT MANE Select	ENSP00000307101.5:p.Pro41LeufsTer13
ENST00000404796.3:c.348-54727_348-54726insAA	ENSP00000385916.2:n.348-54727_348-54726insAA
ENST00000579755.2:c.194-3499_194-3498insTT MANE Plus Clinical	ENSP00000462950.1:n.194-3499_194-3498insTT
ENST00000304494.9:c.121_122insTT	ENSP00000307101.5:p.Pro41LeufsTer13
ENST00000361570.4:c.194-3499_194-3498insTT	ENSP00000355153.4:n.194-3499_194-3498insTT
ENST00000380151.3:c.121_122insTT	ENSP00000369496.3:p.Pro41LeufsTer?
ENST00000404796.2:c.348-54727_348-54726insAA	ENSP00000385916.2:n.348-54727_348-54726insAA
ENST00000494262.5:c.-3-3499_-3-3498insTT	ENSP00000464952.1:n.-3-3499_-3-3498insTT
ENST00000498124.1:c.121_122insTT	ENSP00000418915.1:p.Pro41LeufsTer13
ENST00000498628.6:c.-3-3499_-3-3498insTT	ENSP00000467857.1:n.-3-3499_-3-3498insTT
ENST00000530628.2:c.194-3499_194-3498insTT	ENSP00000432664.2:n.194-3499_194-3498insTT
ENST00000579122.1:c.121_122insTT	ENSP00000464202.1:p.Pro41LeufsTer13
ENST00000579755.1:c.194-3499_194-3498insTT	ENSP00000462950.1:n.194-3499_194-3498insTT
NM_000077.4:c.121_122insTT , LRG_11t1:c.121_122insTT	NP_000068.1:p.Pro41LeufsTer13
NM_001195132.1:c.121_122insTT	NP_001182061.1:p.Pro41LeufsTer13
NM_058195.3:c.194-3499_194-3498insTT , LRG_11t2:c.194-3499_194-3498insTT	NP_478102.2:n.194-3499_194-3498insTT
NM_058197.4:c.121_122insTT	NP_478104.2:p.Pro41LeufsTer?
XM_011517675.1:c.121_122insTT	XP_011515977.1:p.Pro41LeufsTer13
XM_011517676.1:c.121_122insTT	XP_011515978.1:p.Pro41LeufsTer13
XM_011517679.1:c.-3-3499_-3-3498insTT	XP_011515981.1:n.-3-3499_-3-3498insTT
XR_929159.1:n.522_523insTT
XR_929161.1:n.341-3499_341-3498insTT
XR_929162.1:n.341-3499_341-3498insTT
XR_929163.1:n.290-3499_290-3498insTT
NM_001363763.1:c.-3-3499_-3-3498insTT	NP_001350692.1:n.-3-3499_-3-3498insTT
XM_011517675.2:c.121_122insTT	XP_011515977.1:p.Pro41LeufsTer13
XM_011517676.2:c.121_122insTT	XP_011515978.1:p.Pro41LeufsTer13
XR_929159.2:n.451_452insTT
NM_001363763.2:c.-3-3499_-3-3498insTT	NP_001350692.1:n.-3-3499_-3-3498insTT
NM_000077.5:c.121_122insTT MANE Select	NP_000068.1:p.Pro41LeufsTer13
NM_001195132.2:c.121_122insTT	NP_001182061.1:p.Pro41LeufsTer13
NM_058195.4:c.194-3499_194-3498insTT MANE Plus Clinical	NP_478102.2:n.194-3499_194-3498insTT
NM_058197.5:c.121_122insTT	NP_478104.2:p.Pro41LeufsTer?