Canonical Allele Identifier: CA918426253

Gene: CDKN2A

Linked Data

• dbSNP Id: rs1587352965

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21988780_21988781insAAGTTGAAATAAAAT , CM000671.2:g.21988780_21988781insAAGTTGAAATAAAAT	GRCh38
NC_000009.11:g.21988779_21988780insAAGTTGAAATAAAAT , CM000671.1:g.21988779_21988780insAAGTTGAAATAAAAT	GRCh37
NC_000009.10:g.21978779_21978780insAAGTTGAAATAAAAT	NCBI36
NG_007485.1:g.10711_10712insATTTTATTTCAACTT , LRG_11:g.10711_10712insATTTTATTTCAACTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000404796.3:c.348-40653_348-40652insAAGTTGAAATAAAAT	ENSP00000385916.2:n.348-40653_348-40652insAAGTTGAAATAAAAT
ENST00000579755.2:c.193+5358_193+5359insATTTTATTTCAACTT MANE Plus Clinical	ENSP00000462950.1:n.193+5358_193+5359insATTTTATTTCAACTT
ENST00000361570.4:c.193+5358_193+5359insATTTTATTTCAACTT	ENSP00000355153.4:n.193+5358_193+5359insATTTTATTTCAACTT
ENST00000404796.2:c.348-40653_348-40652insAAGTTGAAATAAAAT	ENSP00000385916.2:n.348-40653_348-40652insAAGTTGAAATAAAAT
ENST00000494262.5:c.-4+5101_-4+5102insATTTTATTTCAACTT	ENSP00000464952.1:n.-4+5101_-4+5102insATTTTATTTCAACTT
ENST00000498628.6:c.-4+6040_-4+6041insATTTTATTTCAACTT	ENSP00000467857.1:n.-4+6040_-4+6041insATTTTATTTCAACTT
ENST00000530628.2:c.193+5358_193+5359insATTTTATTTCAACTT	ENSP00000432664.2:n.193+5358_193+5359insATTTTATTTCAACTT
ENST00000579755.1:c.193+5358_193+5359insATTTTATTTCAACTT	ENSP00000462950.1:n.193+5358_193+5359insATTTTATTTCAACTT
NM_058195.3:c.193+5358_193+5359insATTTTATTTCAACTT , LRG_11t2:c.193+5358_193+5359insATTTTATTTCAACTT	NP_478102.2:n.193+5358_193+5359insATTTTATTTCAACTT
XM_011517678.1:c.*1149_*1150insATTTTATTTCAACTT	XP_011515980.1:n.*1149_*1150insATTTTATTTCAACTT
XM_011517679.1:c.-4+6040_-4+6041insATTTTATTTCAACTT	XP_011515981.1:n.-4+6040_-4+6041insATTTTATTTCAACTT
XR_929161.1:n.340+5358_340+5359insATTTTATTTCAACTT
XR_929162.1:n.340+5358_340+5359insATTTTATTTCAACTT
XR_929163.1:n.289+5358_289+5359insATTTTATTTCAACTT
NM_001363763.1:c.-4+6040_-4+6041insATTTTATTTCAACTT	NP_001350692.1:n.-4+6040_-4+6041insATTTTATTTCAACTT
NM_001363763.2:c.-4+6040_-4+6041insATTTTATTTCAACTT	NP_001350692.1:n.-4+6040_-4+6041insATTTTATTTCAACTT
NM_058195.4:c.193+5358_193+5359insATTTTATTTCAACTT MANE Plus Clinical	NP_478102.2:n.193+5358_193+5359insATTTTATTTCAACTT