Canonical Allele Identifier: CA398978981

Gene: ADAP2

Linked Data

• MyVariant Identifiers: chr17:g.29283272A>G (hg19) ; chr17:g.30956254A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.30956254A>G , CM000679.2:g.30956254A>G	GRCh38
NC_000017.10:g.29283272A>G , CM000679.1:g.29283272A>G	GRCh37
NC_000017.9:g.26307398A>G	NCBI36
NG_051975.1:g.39519A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330889.8:c.896A>G MANE Select	ENSP00000329468.3:p.Gln299Arg
ENST00000330889.7:c.896A>G	ENSP00000329468.3:p.Gln299Arg
ENST00000470962.1:n.316A>G
ENST00000480980.1:n.330A>G
ENST00000580525.5:c.914A>G	ENSP00000464121.1:p.Gln305Arg
ENST00000581285.5:c.812A>G	ENSP00000464155.1:p.Gln271Arg
ENST00000584828.5:c.265A>G
ENST00000584989.1:c.188A>G	ENSP00000462634.1:p.Gln63Arg
ENST00000585130.5:c.*495A>G	ENSP00000464120.1:n.*495A>G
NM_018404.2:c.896A>G	NP_060874.1:p.Gln299Arg
XM_005258008.2:c.914A>G	XP_005258065.1:p.Gln305Arg
XM_005258011.2:c.851A>G	XP_005258068.1:p.Gln284Arg
XM_006721973.2:c.914A>G	XP_006722036.1:p.Gln305Arg
XM_011524993.1:c.911A>G	XP_011523295.1:p.Gln304Arg
XM_011524994.1:c.893A>G	XP_011523296.1:p.Gln298Arg
NM_001346712.1:c.914A>G	NP_001333641.1:p.Gln305Arg
NM_001346714.1:c.893A>G	NP_001333643.1:p.Gln298Arg
NM_001346716.1:c.896A>G	NP_001333645.1:p.Gln299Arg
NR_144488.1:n.1095A>G
XM_024450831.1:c.896A>G	XP_024306599.1:p.Gln299Arg
XM_024450832.1:c.911A>G	XP_024306600.1:p.Gln304Arg
XM_024450833.1:c.851A>G	XP_024306601.1:p.Gln284Arg
XM_024450834.1:c.914A>G	XP_024306602.1:p.Gln305Arg
XM_024450835.1:c.530A>G	XP_024306603.1:p.Gln177Arg
NM_018404.3:c.896A>G MANE Select	NP_060874.1:p.Gln299Arg
NM_001346712.2:c.914A>G	NP_001333641.1:p.Gln305Arg
NM_001346714.2:c.893A>G	NP_001333643.1:p.Gln298Arg
NM_001346716.2:c.896A>G	NP_001333645.1:p.Gln299Arg
NR_144488.2:n.886A>G