Canonical Allele Identifier: CA398979640

Gene: ADAP2

Linked Data

• MyVariant Identifiers: chr17:g.29283478A>G (hg19) ; chr17:g.30956460A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.30956460A>G , CM000679.2:g.30956460A>G	GRCh38
NC_000017.10:g.29283478A>G , CM000679.1:g.29283478A>G	GRCh37
NC_000017.9:g.26307604A>G	NCBI36
NG_051975.1:g.39725A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330889.8:c.1102A>G MANE Select	ENSP00000329468.3:p.Asn368Asp
ENST00000330889.7:c.1102A>G	ENSP00000329468.3:p.Asn368Asp
ENST00000470962.1:n.522A>G
ENST00000480980.1:n.536A>G
ENST00000580525.5:c.1120A>G	ENSP00000464121.1:p.Asn374Asp
ENST00000584828.5:c.402+69A>G
ENST00000585130.5:c.*701A>G	ENSP00000464120.1:n.*701A>G
NM_018404.2:c.1102A>G	NP_060874.1:p.Asn368Asp
XM_005258008.2:c.1120A>G	XP_005258065.1:p.Asn374Asp
XM_005258011.2:c.1057A>G	XP_005258068.1:p.Asn353Asp
XM_006721973.2:c.1051+69A>G	XP_006722036.1:n.1051+69A>G
XM_011524993.1:c.1117A>G	XP_011523295.1:p.Asn373Asp
XM_011524994.1:c.1099A>G	XP_011523296.1:p.Asn367Asp
NM_001346712.1:c.1120A>G	NP_001333641.1:p.Asn374Asp
NM_001346714.1:c.1099A>G	NP_001333643.1:p.Asn367Asp
NM_001346716.1:c.1033+69A>G	NP_001333645.1:n.1033+69A>G
NR_144488.1:n.1301A>G
XM_024450831.1:c.1102A>G	XP_024306599.1:p.Asn368Asp
XM_024450832.1:c.1117A>G	XP_024306600.1:p.Asn373Asp
XM_024450833.1:c.1057A>G	XP_024306601.1:p.Asn353Asp
XM_024450834.1:c.1051+69A>G	XP_024306602.1:n.1051+69A>G
XM_024450835.1:c.736A>G	XP_024306603.1:p.Asn246Asp
NM_018404.3:c.1102A>G MANE Select	NP_060874.1:p.Asn368Asp
NM_001346712.2:c.1120A>G	NP_001333641.1:p.Asn374Asp
NM_001346714.2:c.1099A>G	NP_001333643.1:p.Asn367Asp
NM_001346716.2:c.1033+69A>G	NP_001333645.1:n.1033+69A>G
NR_144488.2:n.1092A>G