Canonical Allele Identifier: CA398978997

Gene: ADAP2

Linked Data

• MyVariant Identifiers: chr17:g.29283278A>G (hg19) ; chr17:g.30956260A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.30956260A>G , CM000679.2:g.30956260A>G	GRCh38
NC_000017.10:g.29283278A>G , CM000679.1:g.29283278A>G	GRCh37
NC_000017.9:g.26307404A>G	NCBI36
NG_051975.1:g.39525A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330889.8:c.902A>G MANE Select	ENSP00000329468.3:p.Gln301Arg
ENST00000330889.7:c.902A>G	ENSP00000329468.3:p.Gln301Arg
ENST00000470962.1:n.322A>G
ENST00000480980.1:n.336A>G
ENST00000580525.5:c.920A>G	ENSP00000464121.1:p.Gln307Arg
ENST00000581285.5:c.818A>G	ENSP00000464155.1:p.Gln273Arg
ENST00000584828.5:c.271A>G
ENST00000584989.1:c.194A>G	ENSP00000462634.1:p.Gln65Arg
ENST00000585130.5:c.*501A>G	ENSP00000464120.1:n.*501A>G
NM_018404.2:c.902A>G	NP_060874.1:p.Gln301Arg
XM_005258008.2:c.920A>G	XP_005258065.1:p.Gln307Arg
XM_005258011.2:c.857A>G	XP_005258068.1:p.Gln286Arg
XM_006721973.2:c.920A>G	XP_006722036.1:p.Gln307Arg
XM_011524993.1:c.917A>G	XP_011523295.1:p.Gln306Arg
XM_011524994.1:c.899A>G	XP_011523296.1:p.Gln300Arg
NM_001346712.1:c.920A>G	NP_001333641.1:p.Gln307Arg
NM_001346714.1:c.899A>G	NP_001333643.1:p.Gln300Arg
NM_001346716.1:c.902A>G	NP_001333645.1:p.Gln301Arg
NR_144488.1:n.1101A>G
XM_024450831.1:c.902A>G	XP_024306599.1:p.Gln301Arg
XM_024450832.1:c.917A>G	XP_024306600.1:p.Gln306Arg
XM_024450833.1:c.857A>G	XP_024306601.1:p.Gln286Arg
XM_024450834.1:c.920A>G	XP_024306602.1:p.Gln307Arg
XM_024450835.1:c.536A>G	XP_024306603.1:p.Gln179Arg
NM_018404.3:c.902A>G MANE Select	NP_060874.1:p.Gln301Arg
NM_001346712.2:c.920A>G	NP_001333641.1:p.Gln307Arg
NM_001346714.2:c.899A>G	NP_001333643.1:p.Gln300Arg
NM_001346716.2:c.902A>G	NP_001333645.1:p.Gln301Arg
NR_144488.2:n.892A>G