Canonical Allele Identifier: CA398979614

Gene: ADAP2

Linked Data

• MyVariant Identifiers: chr17:g.29283470C>G (hg19) ; chr17:g.30956452C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.30956452C>G , CM000679.2:g.30956452C>G	GRCh38
NC_000017.10:g.29283470C>G , CM000679.1:g.29283470C>G	GRCh37
NC_000017.9:g.26307596C>G	NCBI36
NG_051975.1:g.39717C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330889.8:c.1094C>G MANE Select	ENSP00000329468.3:p.Thr365Arg
ENST00000330889.7:c.1094C>G	ENSP00000329468.3:p.Thr365Arg
ENST00000470962.1:n.514C>G
ENST00000480980.1:n.528C>G
ENST00000580525.5:c.1112C>G	ENSP00000464121.1:p.Thr371Arg
ENST00000584828.5:c.402+61C>G
ENST00000585130.5:c.*693C>G	ENSP00000464120.1:n.*693C>G
NM_018404.2:c.1094C>G	NP_060874.1:p.Thr365Arg
XM_005258008.2:c.1112C>G	XP_005258065.1:p.Thr371Arg
XM_005258011.2:c.1049C>G	XP_005258068.1:p.Thr350Arg
XM_006721973.2:c.1051+61C>G	XP_006722036.1:n.1051+61C>G
XM_011524993.1:c.1109C>G	XP_011523295.1:p.Thr370Arg
XM_011524994.1:c.1091C>G	XP_011523296.1:p.Thr364Arg
NM_001346712.1:c.1112C>G	NP_001333641.1:p.Thr371Arg
NM_001346714.1:c.1091C>G	NP_001333643.1:p.Thr364Arg
NM_001346716.1:c.1033+61C>G	NP_001333645.1:n.1033+61C>G
NR_144488.1:n.1293C>G
XM_024450831.1:c.1094C>G	XP_024306599.1:p.Thr365Arg
XM_024450832.1:c.1109C>G	XP_024306600.1:p.Thr370Arg
XM_024450833.1:c.1049C>G	XP_024306601.1:p.Thr350Arg
XM_024450834.1:c.1051+61C>G	XP_024306602.1:n.1051+61C>G
XM_024450835.1:c.728C>G	XP_024306603.1:p.Thr243Arg
NM_018404.3:c.1094C>G MANE Select	NP_060874.1:p.Thr365Arg
NM_001346712.2:c.1112C>G	NP_001333641.1:p.Thr371Arg
NM_001346714.2:c.1091C>G	NP_001333643.1:p.Thr364Arg
NM_001346716.2:c.1033+61C>G	NP_001333645.1:n.1033+61C>G
NR_144488.2:n.1084C>G