Canonical Allele Identifier: CA862183557

Gene: CDKN2A

Linked Data

• dbSNP Id: rs1358103564
• MyVariant Identifiers: chr9:g.21989040_21989041insT (hg19) ; chr9:g.21989041_21989042insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21989042dup , CM000671.2:g.21989042dup	GRCh38
NC_000009.11:g.21989041dup , CM000671.1:g.21989041dup	GRCh37
NC_000009.10:g.21979041dup	NCBI36
NG_007485.1:g.10450dup , LRG_11:g.10450dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000404796.3:c.348-40391dup	ENSP00000385916.2:n.348-40391dup
ENST00000579755.2:c.193+5097dup MANE Plus Clinical	ENSP00000462950.1:n.193+5097dup
ENST00000361570.4:c.193+5097dup	ENSP00000355153.4:n.193+5097dup
ENST00000404796.2:c.348-40391dup	ENSP00000385916.2:n.348-40391dup
ENST00000494262.5:c.-4+4840dup	ENSP00000464952.1:n.-4+4840dup
ENST00000498628.6:c.-4+5779dup	ENSP00000467857.1:n.-4+5779dup
ENST00000530628.2:c.193+5097dup	ENSP00000432664.2:n.193+5097dup
ENST00000579755.1:c.193+5097dup	ENSP00000462950.1:n.193+5097dup
NM_058195.3:c.193+5097dup , LRG_11t2:c.193+5097dup	NP_478102.2:n.193+5097dup
XM_011517678.1:c.*888dup	XP_011515980.1:n.*888dup
XM_011517679.1:c.-4+5779dup	XP_011515981.1:n.-4+5779dup
XR_929161.1:n.340+5097dup
XR_929162.1:n.340+5097dup
XR_929163.1:n.289+5097dup
NM_001363763.1:c.-4+5779dup	NP_001350692.1:n.-4+5779dup
NM_001363763.2:c.-4+5779dup	NP_001350692.1:n.-4+5779dup
NM_058195.4:c.193+5097dup MANE Plus Clinical	NP_478102.2:n.193+5097dup