Canonical Allele Identifier: CA464261810

Gene: CDKN2A

Linked Data

• MyVariant Identifiers: chr9:g.21970955_21970956insA (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21970956_21970957insA , CM000671.2:g.21970956_21970957insA	GRCh38
NC_000009.11:g.21970955_21970956insA , CM000671.1:g.21970955_21970956insA	GRCh37
NC_000009.10:g.21960955_21960956insA	NCBI36
NG_007485.1:g.28535_28536insT , LRG_11:g.28535_28536insT

Transcript Alleles

HGVS	Amino-acid change
ENST00000304494.10:c.402_403insT MANE Select	ENSP00000307101.5:p.Gly135TrpfsTer7
ENST00000404796.3:c.348-58477_348-58476insA	ENSP00000385916.2:n.348-58477_348-58476in...
ENST00000579755.2:c.*46_*47insT MANE Plus Clinical	ENSP00000462950.1:n.*46_*47insT
ENST00000304494.9:c.402_403insT	ENSP00000307101.5:p.Gly135TrpfsTer7
ENST00000361570.4:c.444_445insT	ENSP00000355153.4:p.Gly149TrpfsTer7
ENST00000380150.2:n.376_377insT
ENST00000380151.3:c.676_677insT	ENSP00000369496.3:n.676_677insT
ENST00000404796.2:c.348-58477_348-58476insA	ENSP00000385916.2:n.348-58477_348-58476in...
ENST00000479692.2:c.249_250insT	ENSP00000466887.1:p.Gly84TrpfsTer7
ENST00000494262.5:c.249_250insT	ENSP00000464952.1:p.Gly84TrpfsTer7
ENST00000497750.1:c.249_250insT	ENSP00000468510.1:p.Gly84TrpfsTer7
ENST00000498124.1:c.402_403insT	ENSP00000418915.1:p.Gly135TrpfsTer7
ENST00000498628.6:c.249_250insT	ENSP00000467857.1:p.Gly84TrpfsTer7
ENST00000530628.2:c.*27+19_*27+20insT	ENSP00000432664.2:n.*27+19_*27+20insT
ENST00000578845.2:c.249_250insT	ENSP00000467390.1:p.Gly84TrpfsTer7
ENST00000579122.1:c.383+19_383+20insT	ENSP00000464202.1:n.383+19_383+20insT
ENST00000579755.1:c.*46_*47insT	ENSP00000462950.1:n.*46_*47insT
NM_000077.4:c.402_403insT , LRG_11t1:c.402_403insT	NP_000068.1:p.Gly135TrpfsTer7
NM_001195132.1:c.402_403insT	NP_001182061.1:p.Gly135TrpfsTer7
NM_058195.3:c.*46_*47insT , LRG_11t2:c.*46_*47insT	NP_478102.2:n.*46_*47insT
NM_058197.4:c.676_677insT	NP_478104.2:n.676_677insT
XM_005251343.1:c.249_250insT	XP_005251400.1:p.Gly84TrpfsTer7
XM_011517675.1:c.402_403insT	XP_011515977.1:p.Gly135TrpfsTer7
XM_011517676.1:c.402_403insT	XP_011515978.1:p.Gly135TrpfsTer7
XM_011517679.1:c.249_250insT	XP_011515981.1:p.Gly84TrpfsTer7
XR_929159.1:n.803_804insT
XR_929161.1:n.592_593insT
XR_929162.1:n.592_593insT
XR_929163.1:n.541_542insT
XR_929164.1:n.324_325insT
NM_001363763.1:c.249_250insT	NP_001350692.1:p.Gly84TrpfsTer7
XM_011517675.2:c.402_403insT	XP_011515977.1:p.Gly135TrpfsTer7
XM_011517676.2:c.402_403insT	XP_011515978.1:p.Gly135TrpfsTer7
XR_929159.2:n.732_733insT
NM_001363763.2:c.249_250insT	NP_001350692.1:p.Gly84TrpfsTer7
NM_000077.5:c.402_403insT MANE Select	NP_000068.1:p.Gly135TrpfsTer7
NM_001195132.2:c.402_403insT	NP_001182061.1:p.Gly135TrpfsTer7
NM_058195.4:c.*46_*47insT MANE Plus Clinical	NP_478102.2:n.*46_*47insT
NM_058197.5:c.*325_*326insT	NP_478104.2:n.*325_*326insT