Canonical Allele Identifier: CA499226068

Gene: ADAP2

Linked Data

• MyVariant Identifiers: chr17:g.29283276C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.30956258C>G , CM000679.2:g.30956258C>G	GRCh38
NC_000017.10:g.29283276C>G , CM000679.1:g.29283276C>G	GRCh37
NC_000017.9:g.26307402C>G	NCBI36
NG_051975.1:g.39523C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330889.8:c.900C>G MANE Select	ENSP00000329468.3:p.Gly300=
ENST00000330889.7:c.900C>G	ENSP00000329468.3:p.Gly300=
ENST00000470962.1:n.320C>G
ENST00000480980.1:n.334C>G
ENST00000580525.5:c.918C>G	ENSP00000464121.1:p.Gly306=
ENST00000581285.5:c.816C>G	ENSP00000464155.1:p.Gly272=
ENST00000584828.5:c.269C>G
ENST00000584989.1:c.192C>G	ENSP00000462634.1:p.Gly64=
ENST00000585130.5:c.*499C>G	ENSP00000464120.1:n.*499C>G
NM_018404.2:c.900C>G	NP_060874.1:p.Gly300=
XM_005258008.2:c.918C>G	XP_005258065.1:p.Gly306=
XM_005258011.2:c.855C>G	XP_005258068.1:p.Gly285=
XM_006721973.2:c.918C>G	XP_006722036.1:p.Gly306=
XM_011524993.1:c.915C>G	XP_011523295.1:p.Gly305=
XM_011524994.1:c.897C>G	XP_011523296.1:p.Gly299=
NM_001346712.1:c.918C>G	NP_001333641.1:p.Gly306=
NM_001346714.1:c.897C>G	NP_001333643.1:p.Gly299=
NM_001346716.1:c.900C>G	NP_001333645.1:p.Gly300=
NR_144488.1:n.1099C>G
XM_024450831.1:c.900C>G	XP_024306599.1:p.Gly300=
XM_024450832.1:c.915C>G	XP_024306600.1:p.Gly305=
XM_024450833.1:c.855C>G	XP_024306601.1:p.Gly285=
XM_024450834.1:c.918C>G	XP_024306602.1:p.Gly306=
XM_024450835.1:c.534C>G	XP_024306603.1:p.Gly178=
NM_018404.3:c.900C>G MANE Select	NP_060874.1:p.Gly300=
NM_001346712.2:c.918C>G	NP_001333641.1:p.Gly306=
NM_001346714.2:c.897C>G	NP_001333643.1:p.Gly299=
NM_001346716.2:c.900C>G	NP_001333645.1:p.Gly300=
NR_144488.2:n.890C>G