Canonical Allele Identifier: CA2255437247

Gene: ADAP2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.30956262_30956263delinsGT , CM000679.2:g.30956262_30956263delinsGT	GRCh38
NC_000017.10:g.29283280_29283281delinsGT , CM000679.1:g.29283280_29283281delinsGT	GRCh37
NC_000017.9:g.26307406_26307407delinsGT	NCBI36
NG_051975.1:g.39527_39528delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330889.8:c.904_905delinsGT MANE Select	ENSP00000329468.3:p.Val302=
ENST00000330889.7:c.904_905delinsGT	ENSP00000329468.3:p.Val302=
ENST00000470962.1:n.324_325delinsGT
ENST00000480980.1:n.338_339delinsGT
ENST00000580525.5:c.922_923delinsGT	ENSP00000464121.1:p.Val308=
ENST00000581285.5:c.820_821delinsGT	ENSP00000464155.1:p.Val274=
ENST00000584828.5:c.273_274delinsGT
ENST00000584989.1:c.196_197delinsGT	ENSP00000462634.1:p.Val66=
ENST00000585130.5:c.*503_*504delinsGT	ENSP00000464120.1:n.*503_*504delinsGT
NM_018404.2:c.904_905delinsGT	NP_060874.1:p.Val302=
XM_005258008.2:c.922_923delinsGT	XP_005258065.1:p.Val308=
XM_005258011.2:c.859_860delinsGT	XP_005258068.1:p.Val287=
XM_006721973.2:c.922_923delinsGT	XP_006722036.1:p.Val308=
XM_011524993.1:c.919_920delinsGT	XP_011523295.1:p.Val307=
XM_011524994.1:c.901_902delinsGT	XP_011523296.1:p.Val301=
NM_001346712.1:c.922_923delinsGT	NP_001333641.1:p.Val308=
NM_001346714.1:c.901_902delinsGT	NP_001333643.1:p.Val301=
NM_001346716.1:c.904_905delinsGT	NP_001333645.1:p.Val302=
NR_144488.1:n.1103_1104delinsGT
XM_024450831.1:c.904_905delinsGT	XP_024306599.1:p.Val302=
XM_024450832.1:c.919_920delinsGT	XP_024306600.1:p.Val307=
XM_024450833.1:c.859_860delinsGT	XP_024306601.1:p.Val287=
XM_024450834.1:c.922_923delinsGT	XP_024306602.1:p.Val308=
XM_024450835.1:c.538_539delinsGT	XP_024306603.1:p.Val180=
NM_018404.3:c.904_905delinsGT MANE Select	NP_060874.1:p.Val302=
NM_001346712.2:c.922_923delinsGT	NP_001333641.1:p.Val308=
NM_001346714.2:c.901_902delinsGT	NP_001333643.1:p.Val301=
NM_001346716.2:c.904_905delinsGT	NP_001333645.1:p.Val302=
NR_144488.2:n.894_895delinsGT