Canonical Allele Identifier: CA499226128

Gene: ADAP2

Linked Data

• MyVariant Identifiers: chr17:g.29283291G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.30956273G>T , CM000679.2:g.30956273G>T	GRCh38
NC_000017.10:g.29283291G>T , CM000679.1:g.29283291G>T	GRCh37
NC_000017.9:g.26307417G>T	NCBI36
NG_051975.1:g.39538G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330889.8:c.915G>T MANE Select	ENSP00000329468.3:p.Gly305=
ENST00000330889.7:c.915G>T	ENSP00000329468.3:p.Gly305=
ENST00000470962.1:n.335G>T
ENST00000480980.1:n.349G>T
ENST00000580525.5:c.933G>T	ENSP00000464121.1:p.Gly311=
ENST00000581285.5:c.831G>T	ENSP00000464155.1:p.Gly277=
ENST00000584828.5:c.284G>T
ENST00000584989.1:c.207G>T	ENSP00000462634.1:p.Gly69=
ENST00000585130.5:c.*514G>T	ENSP00000464120.1:n.*514G>T
NM_018404.2:c.915G>T	NP_060874.1:p.Gly305=
XM_005258008.2:c.933G>T	XP_005258065.1:p.Gly311=
XM_005258011.2:c.870G>T	XP_005258068.1:p.Gly290=
XM_006721973.2:c.933G>T	XP_006722036.1:p.Gly311=
XM_011524993.1:c.930G>T	XP_011523295.1:p.Gly310=
XM_011524994.1:c.912G>T	XP_011523296.1:p.Gly304=
NM_001346712.1:c.933G>T	NP_001333641.1:p.Gly311=
NM_001346714.1:c.912G>T	NP_001333643.1:p.Gly304=
NM_001346716.1:c.915G>T	NP_001333645.1:p.Gly305=
NR_144488.1:n.1114G>T
XM_024450831.1:c.915G>T	XP_024306599.1:p.Gly305=
XM_024450832.1:c.930G>T	XP_024306600.1:p.Gly310=
XM_024450833.1:c.870G>T	XP_024306601.1:p.Gly290=
XM_024450834.1:c.933G>T	XP_024306602.1:p.Gly311=
XM_024450835.1:c.549G>T	XP_024306603.1:p.Gly183=
NM_018404.3:c.915G>T MANE Select	NP_060874.1:p.Gly305=
NM_001346712.2:c.933G>T	NP_001333641.1:p.Gly311=
NM_001346714.2:c.912G>T	NP_001333643.1:p.Gly304=
NM_001346716.2:c.915G>T	NP_001333645.1:p.Gly305=
NR_144488.2:n.905G>T