Canonical Allele Identifier: CA2783190639

Gene: CDKN2A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21975164_21975165insTTGCAG , CM000671.2:g.21975164_21975165insTTGCAG	GRCh38
NC_000009.11:g.21975163_21975164insTTGCAG , CM000671.1:g.21975163_21975164insTTGCAG	GRCh37
NC_000009.10:g.21965163_21965164insTTGCAG	NCBI36
NG_007485.1:g.24327_24328insCTGCAA , LRG_11:g.24327_24328insCTGCAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000404796.3:c.348-54269_348-54268insTTGCAG	ENSP00000385916.2:n.348-54269_348-54268insTTGCAG
ENST00000579755.2:c.194-3957_194-3956insCTGCAA MANE Plus Clinical	ENSP00000462950.1:n.194-3957_194-3956insCTGCAA
ENST00000361570.4:c.194-3957_194-3956insCTGCAA	ENSP00000355153.4:n.194-3957_194-3956insCTGCAA
ENST00000404796.2:c.348-54269_348-54268insTTGCAG	ENSP00000385916.2:n.348-54269_348-54268insTTGCAG
ENST00000494262.5:c.-3-3957_-3-3956insCTGCAA	ENSP00000464952.1:n.-3-3957_-3-3956insCTGCAA
ENST00000498628.6:c.-3-3957_-3-3956insCTGCAA	ENSP00000467857.1:n.-3-3957_-3-3956insCTGCAA
ENST00000530628.2:c.194-3957_194-3956insCTGCAA	ENSP00000432664.2:n.194-3957_194-3956insCTGCAA
ENST00000579755.1:c.194-3957_194-3956insCTGCAA	ENSP00000462950.1:n.194-3957_194-3956insCTGCAA
NM_058195.3:c.194-3957_194-3956insCTGCAA , LRG_11t2:c.194-3957_194-3956insCTGCAA	NP_478102.2:n.194-3957_194-3956insCTGCAA
XM_011517675.1:c.-338_-337insCTGCAA	XP_011515977.1:n.-338_-337insCTGCAA
XM_011517676.1:c.-338_-337insCTGCAA	XP_011515978.1:n.-338_-337insCTGCAA
XM_011517679.1:c.-3-3957_-3-3956insCTGCAA	XP_011515981.1:n.-3-3957_-3-3956insCTGCAA
XR_929159.1:n.64_65insCTGCAA
XR_929161.1:n.341-3957_341-3956insCTGCAA
XR_929162.1:n.341-3957_341-3956insCTGCAA
XR_929163.1:n.290-3957_290-3956insCTGCAA
NM_001363763.1:c.-3-3957_-3-3956insCTGCAA	NP_001350692.1:n.-3-3957_-3-3956insCTGCAA
NM_001363763.2:c.-3-3957_-3-3956insCTGCAA	NP_001350692.1:n.-3-3957_-3-3956insCTGCAA
NM_058195.4:c.194-3957_194-3956insCTGCAA MANE Plus Clinical	NP_478102.2:n.194-3957_194-3956insCTGCAA