Canonical Allele Identifier: CA499227248

Gene: ADAP2

Linked Data

• MyVariant Identifiers: chr17:g.29283438A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.30956420A>G , CM000679.2:g.30956420A>G	GRCh38
NC_000017.10:g.29283438A>G , CM000679.1:g.29283438A>G	GRCh37
NC_000017.9:g.26307564A>G	NCBI36
NG_051975.1:g.39685A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330889.8:c.1062A>G MANE Select	ENSP00000329468.3:p.Glu354=
ENST00000330889.7:c.1062A>G	ENSP00000329468.3:p.Glu354=
ENST00000470962.1:n.482A>G
ENST00000480980.1:n.496A>G
ENST00000580525.5:c.1080A>G	ENSP00000464121.1:p.Glu360=
ENST00000581285.5:c.978A>G	ENSP00000464155.1:p.Glu326=
ENST00000584828.5:c.402+29A>G
ENST00000585130.5:c.*661A>G	ENSP00000464120.1:n.*661A>G
NM_018404.2:c.1062A>G	NP_060874.1:p.Glu354=
XM_005258008.2:c.1080A>G	XP_005258065.1:p.Glu360=
XM_005258011.2:c.1017A>G	XP_005258068.1:p.Glu339=
XM_006721973.2:c.1051+29A>G	XP_006722036.1:n.1051+29A>G
XM_011524993.1:c.1077A>G	XP_011523295.1:p.Glu359=
XM_011524994.1:c.1059A>G	XP_011523296.1:p.Glu353=
NM_001346712.1:c.1080A>G	NP_001333641.1:p.Glu360=
NM_001346714.1:c.1059A>G	NP_001333643.1:p.Glu353=
NM_001346716.1:c.1033+29A>G	NP_001333645.1:n.1033+29A>G
NR_144488.1:n.1261A>G
XM_024450831.1:c.1062A>G	XP_024306599.1:p.Glu354=
XM_024450832.1:c.1077A>G	XP_024306600.1:p.Glu359=
XM_024450833.1:c.1017A>G	XP_024306601.1:p.Glu339=
XM_024450834.1:c.1051+29A>G	XP_024306602.1:n.1051+29A>G
XM_024450835.1:c.696A>G	XP_024306603.1:p.Glu232=
NM_018404.3:c.1062A>G MANE Select	NP_060874.1:p.Glu354=
NM_001346712.2:c.1080A>G	NP_001333641.1:p.Glu360=
NM_001346714.2:c.1059A>G	NP_001333643.1:p.Glu353=
NM_001346716.2:c.1033+29A>G	NP_001333645.1:n.1033+29A>G
NR_144488.2:n.1052A>G