Canonical Allele Identifier: CA2689599455

Gene: CDKN2A

Linked Data

• gnomAD v4: 9-21975016-G-GT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21975016_21975017insT , CM000671.2:g.21975016_21975017insT	GRCh38
NC_000009.11:g.21975015_21975016insT , CM000671.1:g.21975015_21975016insT	GRCh37
NC_000009.10:g.21965015_21965016insT	NCBI36
NG_007485.1:g.24475_24476insA , LRG_11:g.24475_24476insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000404796.3:c.348-54417_348-54416insT	ENSP00000385916.2:n.348-54417_348-54416insT
ENST00000579755.2:c.194-3809_194-3808insA MANE Plus Clinical	ENSP00000462950.1:n.194-3809_194-3808insA
ENST00000304494.9:c.-190_-189insA	ENSP00000307101.5:n.-190_-189insA
ENST00000361570.4:c.194-3809_194-3808insA	ENSP00000355153.4:n.194-3809_194-3808insA
ENST00000404796.2:c.348-54417_348-54416insT	ENSP00000385916.2:n.348-54417_348-54416insT
ENST00000494262.5:c.-3-3809_-3-3808insA	ENSP00000464952.1:n.-3-3809_-3-3808insA
ENST00000498628.6:c.-3-3809_-3-3808insA	ENSP00000467857.1:n.-3-3809_-3-3808insA
ENST00000530628.2:c.194-3809_194-3808insA	ENSP00000432664.2:n.194-3809_194-3808insA
ENST00000579755.1:c.194-3809_194-3808insA	ENSP00000462950.1:n.194-3809_194-3808insA
NM_000077.4:c.-190_-189insA , LRG_11t1:c.-190_-189insA	NP_000068.1:n.-190_-189insA
NM_001195132.1:c.-190_-189insA	NP_001182061.1:n.-190_-189insA
NM_058195.3:c.194-3809_194-3808insA , LRG_11t2:c.194-3809_194-3808insA	NP_478102.2:n.194-3809_194-3808insA
XM_011517675.1:c.-190_-189insA	XP_011515977.1:n.-190_-189insA
XM_011517676.1:c.-190_-189insA	XP_011515978.1:n.-190_-189insA
XM_011517679.1:c.-3-3809_-3-3808insA	XP_011515981.1:n.-3-3809_-3-3808insA
XR_929159.1:n.212_213insA
XR_929161.1:n.341-3809_341-3808insA
XR_929162.1:n.341-3809_341-3808insA
XR_929163.1:n.290-3809_290-3808insA
NM_001363763.1:c.-3-3809_-3-3808insA	NP_001350692.1:n.-3-3809_-3-3808insA
XM_011517675.2:c.-190_-189insA	XP_011515977.1:n.-190_-189insA
XM_011517676.2:c.-190_-189insA	XP_011515978.1:n.-190_-189insA
XR_929159.2:n.141_142insA
NM_001363763.2:c.-3-3809_-3-3808insA	NP_001350692.1:n.-3-3809_-3-3808insA
NM_058195.4:c.194-3809_194-3808insA MANE Plus Clinical	NP_478102.2:n.194-3809_194-3808insA