Canonical Allele Identifier: CA499229134

Gene: ADAP2

Linked Data

• MyVariant Identifiers: chr17:g.29283873T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.30956855T>G , CM000679.2:g.30956855T>G	GRCh38
NC_000017.10:g.29283873T>G , CM000679.1:g.29283873T>G	GRCh37
NC_000017.9:g.26307999T>G	NCBI36
NG_051975.1:g.40120T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330889.8:c.1111+386T>G MANE Select	ENSP00000329468.3:n.1111+386T>G
ENST00000330889.7:c.1111+386T>G	ENSP00000329468.3:n.1111+386T>G
ENST00000470962.1:n.531+386T>G
ENST00000580525.5:c.1129+386T>G	ENSP00000464121.1:n.1129+386T>G
ENST00000584828.5:c.402+464T>G
ENST00000585130.5:c.*710+386T>G	ENSP00000464120.1:n.*710+386T>G
NM_018404.2:c.1111+386T>G	NP_060874.1:n.1111+386T>G
XM_005258008.2:c.1129+386T>G	XP_005258065.1:n.1129+386T>G
XM_005258011.2:c.1066+386T>G	XP_005258068.1:n.1066+386T>G
XM_006721973.2:c.1051+464T>G	XP_006722036.1:n.1051+464T>G
XM_011524993.1:c.1126+386T>G	XP_011523295.1:n.1126+386T>G
XM_011524994.1:c.1108+386T>G	XP_011523296.1:n.1108+386T>G
NM_001346712.1:c.1129+386T>G	NP_001333641.1:n.1129+386T>G
NM_001346714.1:c.1108+386T>G	NP_001333643.1:n.1108+386T>G
NM_001346716.1:c.1033+464T>G	NP_001333645.1:n.1033+464T>G
NR_144488.1:n.1310+386T>G
XM_024450832.1:c.1126+386T>G	XP_024306600.1:n.1126+386T>G
XM_024450833.1:c.1066+386T>G	XP_024306601.1:n.1066+386T>G
XM_024450834.1:c.1051+464T>G	XP_024306602.1:n.1051+464T>G
XM_024450835.1:c.745+386T>G	XP_024306603.1:n.745+386T>G
NM_018404.3:c.1111+386T>G MANE Select	NP_060874.1:n.1111+386T>G
NM_001346712.2:c.1129+386T>G	NP_001333641.1:n.1129+386T>G
NM_001346714.2:c.1108+386T>G	NP_001333643.1:n.1108+386T>G
NM_001346716.2:c.1033+464T>G	NP_001333645.1:n.1033+464T>G
NR_144488.2:n.1101+386T>G