Canonical Allele Identifier: CA1839161756

Gene: CDKN2A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21971096_21971097delinsTC , CM000671.2:g.21971096_21971097delinsTC	GRCh38
NC_000009.11:g.21971095_21971096delinsTC , CM000671.1:g.21971095_21971096delinsTC	GRCh37
NC_000009.10:g.21961095_21961096delinsTC	NCBI36
NG_007485.1:g.28395_28396delinsGA , LRG_11:g.28395_28396delinsGA

Transcript Alleles

HGVS	Amino-acid change
ENST00000304494.10:c.262_263delinsGA MANE Select	ENSP00000307101.5:p.Glu88=
ENST00000404796.3:c.348-58337_348-58336delinsTC	ENSP00000385916.2:n.348-58337_348-58336de...
ENST00000579755.2:c.305_306delinsGA MANE Plus Clinical	ENSP00000462950.1:p.Gly102=
ENST00000304494.9:c.262_263delinsGA	ENSP00000307101.5:p.Glu88=
ENST00000361570.4:c.304_305delinsGA	ENSP00000355153.4:p.Glu102=
ENST00000380150.2:n.236_237delinsGA
ENST00000380151.3:c.536_537delinsGA	ENSP00000369496.3:n.536_537delinsGA
ENST00000404796.2:c.348-58337_348-58336delinsTC	ENSP00000385916.2:n.348-58337_348-58336de...
ENST00000479692.2:c.109_110delinsGA	ENSP00000466887.1:p.Glu37=
ENST00000494262.5:c.109_110delinsGA	ENSP00000464952.1:p.Glu37=
ENST00000497750.1:c.109_110delinsGA	ENSP00000468510.1:p.Glu37=
ENST00000498124.1:c.262_263delinsGA	ENSP00000418915.1:p.Glu88=
ENST00000498628.6:c.109_110delinsGA	ENSP00000467857.1:p.Glu37=
ENST00000530628.2:c.305_306delinsGA	ENSP00000432664.2:p.Gly102=
ENST00000578845.2:c.109_110delinsGA	ENSP00000467390.1:p.Glu37=
ENST00000579122.1:c.262_263delinsGA	ENSP00000464202.1:p.Glu88=
ENST00000579755.1:c.305_306delinsGA	ENSP00000462950.1:p.Gly102=
NM_000077.4:c.262_263delinsGA , LRG_11t1:c.262_263delinsGA	NP_000068.1:p.Glu88=
NM_001195132.1:c.262_263delinsGA	NP_001182061.1:p.Glu88=
NM_058195.3:c.305_306delinsGA , LRG_11t2:c.305_306delinsGA	NP_478102.2:p.Gly102=
NM_058197.4:c.536_537delinsGA	NP_478104.2:n.536_537delinsGA
XM_005251343.1:c.109_110delinsGA	XP_005251400.1:p.Glu37=
XM_011517675.1:c.262_263delinsGA	XP_011515977.1:p.Glu88=
XM_011517676.1:c.262_263delinsGA	XP_011515978.1:p.Glu88=
XM_011517679.1:c.109_110delinsGA	XP_011515981.1:p.Glu37=
XR_929159.1:n.663_664delinsGA
XR_929161.1:n.452_453delinsGA
XR_929162.1:n.452_453delinsGA
XR_929163.1:n.401_402delinsGA
XR_929164.1:n.184_185delinsGA
NM_001363763.1:c.109_110delinsGA	NP_001350692.1:p.Glu37=
XM_011517675.2:c.262_263delinsGA	XP_011515977.1:p.Glu88=
XM_011517676.2:c.262_263delinsGA	XP_011515978.1:p.Glu88=
XR_929159.2:n.592_593delinsGA
NM_001363763.2:c.109_110delinsGA	NP_001350692.1:p.Glu37=
NM_000077.5:c.262_263delinsGA MANE Select	NP_000068.1:p.Glu88=
NM_001195132.2:c.262_263delinsGA	NP_001182061.1:p.Glu88=
NM_058195.4:c.305_306delinsGA MANE Plus Clinical	NP_478102.2:p.Gly102=
NM_058197.5:c.*185_*186delinsGA	NP_478104.2:n.*185_*186delinsGA