Canonical Allele Identifier: CA1839173832

Gene: CDKN2A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21974917_21974920delinsCCCT , CM000671.2:g.21974917_21974920delinsCCCT	GRCh38
NC_000009.11:g.21974916_21974919delinsCCCT , CM000671.1:g.21974916_21974919delinsCCCT	GRCh37
NC_000009.10:g.21964916_21964919delinsCCCT	NCBI36
NG_007485.1:g.24572_24575delinsAGGG , LRG_11:g.24572_24575delinsAGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000404796.3:c.348-54516_348-54513delinsCCCT	ENSP00000385916.2:n.348-54516_348-54513delinsCCCT
ENST00000579755.2:c.194-3712_194-3709delinsAGGG MANE Plus Clinical	ENSP00000462950.1:n.194-3712_194-3709delinsAGGG
ENST00000304494.9:c.-93_-90delinsAGGG	ENSP00000307101.5:n.-93_-90delinsAGGG
ENST00000361570.4:c.194-3712_194-3709delinsAGGG	ENSP00000355153.4:n.194-3712_194-3709delinsAGGG
ENST00000404796.2:c.348-54516_348-54513delinsCCCT	ENSP00000385916.2:n.348-54516_348-54513delinsCCCT
ENST00000494262.5:c.-3-3712_-3-3709delinsAGGG	ENSP00000464952.1:n.-3-3712_-3-3709delinsAGGG
ENST00000498628.6:c.-3-3712_-3-3709delinsAGGG	ENSP00000467857.1:n.-3-3712_-3-3709delinsAGGG
ENST00000530628.2:c.194-3712_194-3709delinsAGGG	ENSP00000432664.2:n.194-3712_194-3709delinsAGGG
ENST00000579755.1:c.194-3712_194-3709delinsAGGG	ENSP00000462950.1:n.194-3712_194-3709delinsAGGG
NM_000077.4:c.-93_-90delinsAGGG , LRG_11t1:c.-93_-90delinsAGGG	NP_000068.1:n.-93_-90delinsAGGG
NM_001195132.1:c.-93_-90delinsAGGG	NP_001182061.1:n.-93_-90delinsAGGG
NM_058195.3:c.194-3712_194-3709delinsAGGG , LRG_11t2:c.194-3712_194-3709delinsAGGG	NP_478102.2:n.194-3712_194-3709delinsAGGG
XM_011517675.1:c.-93_-90delinsAGGG	XP_011515977.1:n.-93_-90delinsAGGG
XM_011517676.1:c.-93_-90delinsAGGG	XP_011515978.1:n.-93_-90delinsAGGG
XM_011517679.1:c.-3-3712_-3-3709delinsAGGG	XP_011515981.1:n.-3-3712_-3-3709delinsAGGG
XR_929159.1:n.309_312delinsAGGG
XR_929161.1:n.341-3712_341-3709delinsAGGG
XR_929162.1:n.341-3712_341-3709delinsAGGG
XR_929163.1:n.290-3712_290-3709delinsAGGG
NM_001363763.1:c.-3-3712_-3-3709delinsAGGG	NP_001350692.1:n.-3-3712_-3-3709delinsAGGG
XM_011517675.2:c.-93_-90delinsAGGG	XP_011515977.1:n.-93_-90delinsAGGG
XM_011517676.2:c.-93_-90delinsAGGG	XP_011515978.1:n.-93_-90delinsAGGG
XR_929159.2:n.238_241delinsAGGG
NM_001363763.2:c.-3-3712_-3-3709delinsAGGG	NP_001350692.1:n.-3-3712_-3-3709delinsAGGG
NM_058195.4:c.194-3712_194-3709delinsAGGG MANE Plus Clinical	NP_478102.2:n.194-3712_194-3709delinsAGGG