Canonical Allele Identifier: CA398978964

Gene: ADAP2

Linked Data

• MyVariant Identifiers: chr17:g.29283265T>A (hg19) ; chr17:g.30956247T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.30956247T>A , CM000679.2:g.30956247T>A	GRCh38
NC_000017.10:g.29283265T>A , CM000679.1:g.29283265T>A	GRCh37
NC_000017.9:g.26307391T>A	NCBI36
NG_051975.1:g.39512T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330889.8:c.889T>A MANE Select	ENSP00000329468.3:p.Phe297Ile
ENST00000330889.7:c.889T>A	ENSP00000329468.3:p.Phe297Ile
ENST00000470962.1:n.309T>A
ENST00000480980.1:n.323T>A
ENST00000580525.5:c.907T>A	ENSP00000464121.1:p.Phe303Ile
ENST00000581285.5:c.805T>A	ENSP00000464155.1:p.Phe269Ile
ENST00000584828.5:c.258T>A
ENST00000584989.1:c.181T>A	ENSP00000462634.1:p.Phe61Ile
ENST00000585130.5:c.*488T>A	ENSP00000464120.1:n.*488T>A
NM_018404.2:c.889T>A	NP_060874.1:p.Phe297Ile
XM_005258008.2:c.907T>A	XP_005258065.1:p.Phe303Ile
XM_005258011.2:c.844T>A	XP_005258068.1:p.Phe282Ile
XM_006721973.2:c.907T>A	XP_006722036.1:p.Phe303Ile
XM_011524993.1:c.904T>A	XP_011523295.1:p.Phe302Ile
XM_011524994.1:c.886T>A	XP_011523296.1:p.Phe296Ile
NM_001346712.1:c.907T>A	NP_001333641.1:p.Phe303Ile
NM_001346714.1:c.886T>A	NP_001333643.1:p.Phe296Ile
NM_001346716.1:c.889T>A	NP_001333645.1:p.Phe297Ile
NR_144488.1:n.1088T>A
XM_024450831.1:c.889T>A	XP_024306599.1:p.Phe297Ile
XM_024450832.1:c.904T>A	XP_024306600.1:p.Phe302Ile
XM_024450833.1:c.844T>A	XP_024306601.1:p.Phe282Ile
XM_024450834.1:c.907T>A	XP_024306602.1:p.Phe303Ile
XM_024450835.1:c.523T>A	XP_024306603.1:p.Phe175Ile
NM_018404.3:c.889T>A MANE Select	NP_060874.1:p.Phe297Ile
NM_001346712.2:c.907T>A	NP_001333641.1:p.Phe303Ile
NM_001346714.2:c.886T>A	NP_001333643.1:p.Phe296Ile
NM_001346716.2:c.889T>A	NP_001333645.1:p.Phe297Ile
NR_144488.2:n.879T>A