Canonical Allele Identifier: CA1259712543

Gene: ADD2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.70747739_70747763delinsCAGCGACAGTATCTCTTTAGGGACT , CM000664.2:g.70747739_70747763delinsCAGCGACAGTATCTCTTTAGGGACT	GRCh38
NC_000002.11:g.70974871_70974895delinsCAGCGACAGTATCTCTTTAGGGACT , CM000664.1:g.70974871_70974895delinsCAGCGACAGTATCTCTTTAGGGACT	GRCh37
NC_000002.10:g.70828379_70828403delinsCAGCGACAGTATCTCTTTAGGGACT	NCBI36
NG_029481.1:g.25481_25505delinsAGTCCCTAAAGAGATACTGTCGCTG
NG_029481.2:g.25481_25505delinsAGTCCCTAAAGAGATACTGTCGCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264436.9:c.-154+20123_-154+20147delinsAGTCCCTAAAGAGATACTGTCGCTG MANE Select	ENSP00000264436.3:n.-154+20123_-154+20147delinsAGTCCCTAAAGAGA...
ENST00000264436.8:c.-154+20123_-154+20147delinsAGTCCCTAAAGAGATACTGTCGCTG	ENSP00000264436.3:n.-154+20123_-154+20147delinsAGTCCCTAAAGAGA...
ENST00000355733.7:c.-154+20123_-154+20147delinsAGTCCCTAAAGAGATACTGTCGCTG	ENSP00000347972.3:n.-154+20123_-154+20147delinsAGTCCCTAAAGAGA...
ENST00000403045.6:c.-154+20123_-154+20147delinsAGTCCCTAAAGAGATACTGTCGCTG	ENSP00000384303.2:n.-154+20123_-154+20147delinsAGTCCCTAAAGAGA...
ENST00000407644.6:c.-154+19841_-154+19865delinsAGTCCCTAAAGAGATACTGTCGCTG	ENSP00000384677.2:n.-154+19841_-154+19865delinsAGTCCCTAAAGAGA...
ENST00000413157.6:c.-154+20123_-154+20147delinsAGTCCCTAAAGAGATACTGTCGCTG	ENSP00000388072.2:n.-154+20123_-154+20147delinsAGTCCCTAAAGAGA...
ENST00000425976.5:c.-154+19567_-154+19591delinsAGTCCCTAAAGAGATACTGTCGCTG	ENSP00000412681.1:n.-154+19567_-154+19591delinsAGTCCCTAAAGAGA...
ENST00000430656.5:c.14+20123_14+20147delinsAGTCCCTAAAGAGATACTGTCGCTG	ENSP00000398112.1:n.14+20123_14+20147delinsAGTCCCTAAAGAGATACT...
ENST00000447731.6:c.-219-6357_-219-6333delinsAGTCCCTAAAGAGATACTGTCGCTG	ENSP00000403722.1:n.-219-6357_-219-6333delinsAGTCCCTAAAGAGATA...
ENST00000473232.1:n.315+20123_315+20147delinsAGTCCCTAAAGAGATACTGTCGCTG
ENST00000496178.1:n.436+12843_436+12867delinsAGTCCCTAAAGAGATACTGTCGCTG
NM_001185054.1:c.-154+19841_-154+19865delinsAGTCCCTAAAGAGATACTGTCGCTG	NP_001171983.1:n.-154+19841_-154+19865delinsAGTCCCTAAAGAGATAC...
NM_001185055.1:c.14+20123_14+20147delinsAGTCCCTAAAGAGATACTGTCGCTG	NP_001171984.1:n.14+20123_14+20147delinsAGTCCCTAAAGAGATACTGTC...
NM_001617.3:c.-154+20123_-154+20147delinsAGTCCCTAAAGAGATACTGTCGCTG	NP_001608.1:n.-154+20123_-154+20147delinsAGTCCCTAAAGAGATACTGT...
NM_017482.3:c.-154+20123_-154+20147delinsAGTCCCTAAAGAGATACTGTCGCTG	NP_059516.2:n.-154+20123_-154+20147delinsAGTCCCTAAAGAGATACTGT...
NM_017488.3:c.-154+20123_-154+20147delinsAGTCCCTAAAGAGATACTGTCGCTG	NP_059522.1:n.-154+20123_-154+20147delinsAGTCCCTAAAGAGATACTGT...
XM_011532503.1:c.-272+20123_-272+20147delinsAGTCCCTAAAGAGATACTGTCGCTG	XP_011530805.1:n.-272+20123_-272+20147delinsAGTCCCTAAAGAGATAC...
NM_001617.4:c.-154+20123_-154+20147delinsAGTCCCTAAAGAGATACTGTCGCTG MANE Select	NP_001608.1:n.-154+20123_-154+20147delinsAGTCCCTAAAGAGATACTGT...
NM_001185055.2:c.14+20123_14+20147delinsAGTCCCTAAAGAGATACTGTCGCTG	NP_001171984.1:n.14+20123_14+20147delinsAGTCCCTAAAGAGATACTGTC...
NM_017482.4:c.-154+20123_-154+20147delinsAGTCCCTAAAGAGATACTGTCGCTG	NP_059516.2:n.-154+20123_-154+20147delinsAGTCCCTAAAGAGATACTGT...
NM_017488.4:c.-154+20123_-154+20147delinsAGTCCCTAAAGAGATACTGTCGCTG	NP_059522.1:n.-154+20123_-154+20147delinsAGTCCCTAAAGAGATACTGT...
NM_001185054.2:c.-154+19841_-154+19865delinsAGTCCCTAAAGAGATACTGTCGCTG	NP_001171983.1:n.-154+19841_-154+19865delinsAGTCCCTAAAGAGATAC...