Canonical Allele Identifier: CA1839171904

Gene: CDKN2A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21974156_21974157delinsGA , CM000671.2:g.21974156_21974157delinsGA	GRCh38
NC_000009.11:g.21974155_21974156delinsGA , CM000671.1:g.21974155_21974156delinsGA	GRCh37
NC_000009.10:g.21964155_21964156delinsGA	NCBI36
NG_007485.1:g.25335_25336delinsTC , LRG_11:g.25335_25336delinsTC

Transcript Alleles

HGVS	Amino-acid change
ENST00000304494.10:c.150+521_150+522delinsTC MANE Select	ENSP00000307101.5:n.150+521_150+522delins...
ENST00000404796.3:c.348-55277_348-55276delinsGA	ENSP00000385916.2:n.348-55277_348-55276de...
ENST00000579755.2:c.194-2949_194-2948delinsTC MANE Plus Clinical	ENSP00000462950.1:n.194-2949_194-2948deli...
ENST00000304494.9:c.150+521_150+522delinsTC	ENSP00000307101.5:n.150+521_150+522delins...
ENST00000361570.4:c.194-2949_194-2948delinsTC	ENSP00000355153.4:n.194-2949_194-2948deli...
ENST00000380151.3:c.424+247_424+248delinsTC	ENSP00000369496.3:n.424+247_424+248delins...
ENST00000404796.2:c.348-55277_348-55276delinsGA	ENSP00000385916.2:n.348-55277_348-55276de...
ENST00000494262.5:c.-3-2949_-3-2948delinsTC	ENSP00000464952.1:n.-3-2949_-3-2948delins...
ENST00000498124.1:c.150+521_150+522delinsTC	ENSP00000418915.1:n.150+521_150+522delins...
ENST00000498628.6:c.-3-2949_-3-2948delinsTC	ENSP00000467857.1:n.-3-2949_-3-2948delins...
ENST00000530628.2:c.194-2949_194-2948delinsTC	ENSP00000432664.2:n.194-2949_194-2948deli...
ENST00000579122.1:c.150+521_150+522delinsTC	ENSP00000464202.1:n.150+521_150+522delins...
ENST00000579755.1:c.194-2949_194-2948delinsTC	ENSP00000462950.1:n.194-2949_194-2948deli...
NM_000077.4:c.150+521_150+522delinsTC , LRG_11t1:c.150+521_150+522delinsTC	NP_000068.1:n.150+521_150+522delinsTC
NM_001195132.1:c.150+521_150+522delinsTC	NP_001182061.1:n.150+521_150+522delinsTC
NM_058195.3:c.194-2949_194-2948delinsTC , LRG_11t2:c.194-2949_194-2948delinsTC	NP_478102.2:n.194-2949_194-2948delinsTC
NM_058197.4:c.424+247_424+248delinsTC	NP_478104.2:n.424+247_424+248delinsTC
XM_011517675.1:c.150+521_150+522delinsTC	XP_011515977.1:n.150+521_150+522delinsTC
XM_011517676.1:c.150+521_150+522delinsTC	XP_011515978.1:n.150+521_150+522delinsTC
XM_011517679.1:c.-3-2949_-3-2948delinsTC	XP_011515981.1:n.-3-2949_-3-2948delinsTC
XR_929159.1:n.551+521_551+522delinsTC
XR_929161.1:n.341-2949_341-2948delinsTC
XR_929162.1:n.341-2949_341-2948delinsTC
XR_929163.1:n.290-2949_290-2948delinsTC
NM_001363763.1:c.-3-2949_-3-2948delinsTC	NP_001350692.1:n.-3-2949_-3-2948delinsTC
XM_011517675.2:c.150+521_150+522delinsTC	XP_011515977.1:n.150+521_150+522delinsTC
XM_011517676.2:c.150+521_150+522delinsTC	XP_011515978.1:n.150+521_150+522delinsTC
XR_929159.2:n.480+521_480+522delinsTC
NM_001363763.2:c.-3-2949_-3-2948delinsTC	NP_001350692.1:n.-3-2949_-3-2948delinsTC
NM_000077.5:c.150+521_150+522delinsTC MANE Select	NP_000068.1:n.150+521_150+522delinsTC
NM_001195132.2:c.150+521_150+522delinsTC	NP_001182061.1:n.150+521_150+522delinsTC
NM_058195.4:c.194-2949_194-2948delinsTC MANE Plus Clinical	NP_478102.2:n.194-2949_194-2948delinsTC
NM_058197.5:c.*73+247_*73+248delinsTC	NP_478104.2:n.*73+247_*73+248delinsTC