Canonical Allele Identifier: CA2255437334

Gene: ADAP2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.30956470_30956471delinsGT , CM000679.2:g.30956470_30956471delinsGT	GRCh38
NC_000017.10:g.29283488_29283489delinsGT , CM000679.1:g.29283488_29283489delinsGT	GRCh37
NC_000017.9:g.26307614_26307615delinsGT	NCBI36
NG_051975.1:g.39735_39736delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330889.8:c.1111+1_1111+2delinsGT MANE Select	ENSP00000329468.3:n.1111+1_1111+2delinsGT
ENST00000330889.7:c.1111+1_1111+2delinsGT	ENSP00000329468.3:n.1111+1_1111+2delinsGT
ENST00000470962.1:n.531+1_531+2delinsGT
ENST00000480980.1:n.546_547delinsGT
ENST00000580525.5:c.1129+1_1129+2delinsGT	ENSP00000464121.1:n.1129+1_1129+2delinsGT
ENST00000584828.5:c.402+79_402+80delinsGT
ENST00000585130.5:c.*710+1_*710+2delinsGT	ENSP00000464120.1:n.*710+1_*710+2delinsGT
NM_018404.2:c.1111+1_1111+2delinsGT	NP_060874.1:n.1111+1_1111+2delinsGT
XM_005258008.2:c.1129+1_1129+2delinsGT	XP_005258065.1:n.1129+1_1129+2delinsGT
XM_005258011.2:c.1066+1_1066+2delinsGT	XP_005258068.1:n.1066+1_1066+2delinsGT
XM_006721973.2:c.1051+79_1051+80delinsGT	XP_006722036.1:n.1051+79_1051+80delinsGT
XM_011524993.1:c.1126+1_1126+2delinsGT	XP_011523295.1:n.1126+1_1126+2delinsGT
XM_011524994.1:c.1108+1_1108+2delinsGT	XP_011523296.1:n.1108+1_1108+2delinsGT
NM_001346712.1:c.1129+1_1129+2delinsGT	NP_001333641.1:n.1129+1_1129+2delinsGT
NM_001346714.1:c.1108+1_1108+2delinsGT	NP_001333643.1:n.1108+1_1108+2delinsGT
NM_001346716.1:c.1033+79_1033+80delinsGT	NP_001333645.1:n.1033+79_1033+80delinsGT
NR_144488.1:n.1310+1_1310+2delinsGT
XM_024450831.1:c.1112_1113delinsGT	XP_024306599.1:p.Ser371=
XM_024450832.1:c.1126+1_1126+2delinsGT	XP_024306600.1:n.1126+1_1126+2delinsGT
XM_024450833.1:c.1066+1_1066+2delinsGT	XP_024306601.1:n.1066+1_1066+2delinsGT
XM_024450834.1:c.1051+79_1051+80delinsGT	XP_024306602.1:n.1051+79_1051+80delinsGT
XM_024450835.1:c.745+1_745+2delinsGT	XP_024306603.1:n.745+1_745+2delinsGT
NM_018404.3:c.1111+1_1111+2delinsGT MANE Select	NP_060874.1:n.1111+1_1111+2delinsGT
NM_001346712.2:c.1129+1_1129+2delinsGT	NP_001333641.1:n.1129+1_1129+2delinsGT
NM_001346714.2:c.1108+1_1108+2delinsGT	NP_001333643.1:n.1108+1_1108+2delinsGT
NM_001346716.2:c.1033+79_1033+80delinsGT	NP_001333645.1:n.1033+79_1033+80delinsGT
NR_144488.2:n.1101+1_1101+2delinsGT