Canonical Allele Identifier: CA1839171805

Gene: CDKN2A

Linked Data

• dbSNP Id: rs1819904492

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21974056_21974058del , CM000671.2:g.21974056_21974058del	GRCh38
NC_000009.11:g.21974055_21974057del , CM000671.1:g.21974055_21974057del	GRCh37
NC_000009.10:g.21964055_21964057del	NCBI36
NG_007485.1:g.25436_25438del , LRG_11:g.25436_25438del

Transcript Alleles

HGVS	Amino-acid change
ENST00000304494.10:c.150+622_150+624del MANE Select	ENSP00000307101.5:n.150+622_150+624del
ENST00000404796.3:c.348-55377_348-55375del	ENSP00000385916.2:n.348-55377_348-55375del
ENST00000579755.2:c.194-2848_194-2846del MANE Plus Clinical	ENSP00000462950.1:n.194-2848_194-2846del
ENST00000304494.9:c.150+622_150+624del	ENSP00000307101.5:n.150+622_150+624del
ENST00000361570.4:c.194-2848_194-2846del	ENSP00000355153.4:n.194-2848_194-2846del
ENST00000380151.3:c.424+348_424+350del	ENSP00000369496.3:n.424+348_424+350del
ENST00000404796.2:c.348-55377_348-55375del	ENSP00000385916.2:n.348-55377_348-55375del
ENST00000494262.5:c.-3-2848_-3-2846del	ENSP00000464952.1:n.-3-2848_-3-2846del
ENST00000498124.1:c.150+622_150+624del	ENSP00000418915.1:n.150+622_150+624del
ENST00000498628.6:c.-3-2848_-3-2846del	ENSP00000467857.1:n.-3-2848_-3-2846del
ENST00000530628.2:c.194-2848_194-2846del	ENSP00000432664.2:n.194-2848_194-2846del
ENST00000579122.1:c.150+622_150+624del	ENSP00000464202.1:n.150+622_150+624del
ENST00000579755.1:c.194-2848_194-2846del	ENSP00000462950.1:n.194-2848_194-2846del
NM_000077.4:c.150+622_150+624del , LRG_11t1:c.150+622_150+624del	NP_000068.1:n.150+622_150+624del
NM_001195132.1:c.150+622_150+624del	NP_001182061.1:n.150+622_150+624del
NM_058195.3:c.194-2848_194-2846del , LRG_11t2:c.194-2848_194-2846del	NP_478102.2:n.194-2848_194-2846del
NM_058197.4:c.424+348_424+350del	NP_478104.2:n.424+348_424+350del
XM_011517675.1:c.150+622_150+624del	XP_011515977.1:n.150+622_150+624del
XM_011517676.1:c.150+622_150+624del	XP_011515978.1:n.150+622_150+624del
XM_011517679.1:c.-3-2848_-3-2846del	XP_011515981.1:n.-3-2848_-3-2846del
XR_929159.1:n.551+622_551+624del
XR_929161.1:n.341-2848_341-2846del
XR_929162.1:n.341-2848_341-2846del
XR_929163.1:n.290-2848_290-2846del
NM_001363763.1:c.-3-2848_-3-2846del	NP_001350692.1:n.-3-2848_-3-2846del
XM_011517675.2:c.150+622_150+624del	XP_011515977.1:n.150+622_150+624del
XM_011517676.2:c.150+622_150+624del	XP_011515978.1:n.150+622_150+624del
XR_929159.2:n.480+622_480+624del
NM_001363763.2:c.-3-2848_-3-2846del	NP_001350692.1:n.-3-2848_-3-2846del
NM_000077.5:c.150+622_150+624del MANE Select	NP_000068.1:n.150+622_150+624del
NM_001195132.2:c.150+622_150+624del	NP_001182061.1:n.150+622_150+624del
NM_058195.4:c.194-2848_194-2846del MANE Plus Clinical	NP_478102.2:n.194-2848_194-2846del
NM_058197.5:c.*73+348_*73+350del	NP_478104.2:n.*73+348_*73+350del