Canonical Allele Identifier: CA398979395

Gene: ADAP2

Linked Data

• gnomAD v4: 17-30956393-T-G
• MyVariant Identifiers: chr17:g.29283411T>G (hg19) ; chr17:g.30956393T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.30956393T>G , CM000679.2:g.30956393T>G	GRCh38
NC_000017.10:g.29283411T>G , CM000679.1:g.29283411T>G	GRCh37
NC_000017.9:g.26307537T>G	NCBI36
NG_051975.1:g.39658T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330889.8:c.1035T>G MANE Select	ENSP00000329468.3:p.Ser345Arg
ENST00000330889.7:c.1035T>G	ENSP00000329468.3:p.Ser345Arg
ENST00000470962.1:n.455T>G
ENST00000480980.1:n.469T>G
ENST00000580525.5:c.1053T>G	ENSP00000464121.1:p.Ser351Arg
ENST00000581285.5:c.951T>G	ENSP00000464155.1:p.Ser317Arg
ENST00000584828.5:c.402+2T>G
ENST00000585130.5:c.*634T>G	ENSP00000464120.1:n.*634T>G
NM_018404.2:c.1035T>G	NP_060874.1:p.Ser345Arg
XM_005258008.2:c.1053T>G	XP_005258065.1:p.Ser351Arg
XM_005258011.2:c.990T>G	XP_005258068.1:p.Ser330Arg
XM_006721973.2:c.1051+2T>G	XP_006722036.1:n.1051+2T>G
XM_011524993.1:c.1050T>G	XP_011523295.1:p.Ser350Arg
XM_011524994.1:c.1032T>G	XP_011523296.1:p.Ser344Arg
NM_001346712.1:c.1053T>G	NP_001333641.1:p.Ser351Arg
NM_001346714.1:c.1032T>G	NP_001333643.1:p.Ser344Arg
NM_001346716.1:c.1033+2T>G	NP_001333645.1:n.1033+2T>G
NR_144488.1:n.1234T>G
XM_024450831.1:c.1035T>G	XP_024306599.1:p.Ser345Arg
XM_024450832.1:c.1050T>G	XP_024306600.1:p.Ser350Arg
XM_024450833.1:c.990T>G	XP_024306601.1:p.Ser330Arg
XM_024450834.1:c.1051+2T>G	XP_024306602.1:n.1051+2T>G
XM_024450835.1:c.669T>G	XP_024306603.1:p.Ser223Arg
NM_018404.3:c.1035T>G MANE Select	NP_060874.1:p.Ser345Arg
NM_001346712.2:c.1053T>G	NP_001333641.1:p.Ser351Arg
NM_001346714.2:c.1032T>G	NP_001333643.1:p.Ser344Arg
NM_001346716.2:c.1033+2T>G	NP_001333645.1:n.1033+2T>G
NR_144488.2:n.1025T>G