Canonical Allele Identifier: CA2695210498

Gene: CDKN2A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21974809_21974813del , CM000671.2:g.21974809_21974813del	GRCh38
NC_000009.11:g.21974808_21974812del , CM000671.1:g.21974808_21974812del	GRCh37
NC_000009.10:g.21964808_21964812del	NCBI36
NG_007485.1:g.24680_24684del , LRG_11:g.24680_24684del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304494.10:c.16_20del MANE Select	ENSP00000307101.5:p.Gly6GlnfsTer7
ENST00000404796.3:c.348-54624_348-54620del	ENSP00000385916.2:n.348-54624_348-54620del
ENST00000579755.2:c.194-3604_194-3600del MANE Plus Clinical	ENSP00000462950.1:n.194-3604_194-3600del
ENST00000304494.9:c.16_20del	ENSP00000307101.5:p.Gly6GlnfsTer7
ENST00000361570.4:c.194-3604_194-3600del	ENSP00000355153.4:n.194-3604_194-3600del
ENST00000380151.3:c.16_20del	ENSP00000369496.3:p.Gly6GlnfsTer7
ENST00000404796.2:c.348-54624_348-54620del	ENSP00000385916.2:n.348-54624_348-54620del
ENST00000494262.5:c.-3-3604_-3-3600del	ENSP00000464952.1:n.-3-3604_-3-3600del
ENST00000498124.1:c.16_20del	ENSP00000418915.1:p.Gly6GlnfsTer7
ENST00000498628.6:c.-3-3604_-3-3600del	ENSP00000467857.1:n.-3-3604_-3-3600del
ENST00000530628.2:c.194-3604_194-3600del	ENSP00000432664.2:n.194-3604_194-3600del
ENST00000579122.1:c.16_20del	ENSP00000464202.1:p.Gly6GlnfsTer7
ENST00000579755.1:c.194-3604_194-3600del	ENSP00000462950.1:n.194-3604_194-3600del
NM_000077.4:c.16_20del , LRG_11t1:c.16_20del	NP_000068.1:p.Gly6GlnfsTer7
NM_001195132.1:c.16_20del	NP_001182061.1:p.Gly6GlnfsTer7
NM_058195.3:c.194-3604_194-3600del , LRG_11t2:c.194-3604_194-3600del	NP_478102.2:n.194-3604_194-3600del
NM_058197.4:c.16_20del	NP_478104.2:p.Gly6GlnfsTer7
XM_011517675.1:c.16_20del	XP_011515977.1:p.Gly6GlnfsTer7
XM_011517676.1:c.16_20del	XP_011515978.1:p.Gly6GlnfsTer7
XM_011517679.1:c.-3-3604_-3-3600del	XP_011515981.1:n.-3-3604_-3-3600del
XR_929159.1:n.417_421del
XR_929161.1:n.341-3604_341-3600del
XR_929162.1:n.341-3604_341-3600del
XR_929163.1:n.290-3604_290-3600del
NM_001363763.1:c.-3-3604_-3-3600del	NP_001350692.1:n.-3-3604_-3-3600del
XM_011517675.2:c.16_20del	XP_011515977.1:p.Gly6GlnfsTer7
XM_011517676.2:c.16_20del	XP_011515978.1:p.Gly6GlnfsTer7
XR_929159.2:n.346_350del
NM_001363763.2:c.-3-3604_-3-3600del	NP_001350692.1:n.-3-3604_-3-3600del
NM_000077.5:c.16_20del MANE Select	NP_000068.1:p.Gly6GlnfsTer7
NM_001195132.2:c.16_20del	NP_001182061.1:p.Gly6GlnfsTer7
NM_058195.4:c.194-3604_194-3600del MANE Plus Clinical	NP_478102.2:n.194-3604_194-3600del
NM_058197.5:c.16_20del	NP_478104.2:p.Gly6GlnfsTer7