Canonical Allele Identifier: CA499227315

Gene: ADAP2

Linked Data

• MyVariant Identifiers: chr17:g.29283453C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.30956435C>T , CM000679.2:g.30956435C>T	GRCh38
NC_000017.10:g.29283453C>T , CM000679.1:g.29283453C>T	GRCh37
NC_000017.9:g.26307579C>T	NCBI36
NG_051975.1:g.39700C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330889.8:c.1077C>T MANE Select	ENSP00000329468.3:p.Val359=
ENST00000330889.7:c.1077C>T	ENSP00000329468.3:p.Val359=
ENST00000470962.1:n.497C>T
ENST00000480980.1:n.511C>T
ENST00000580525.5:c.1095C>T	ENSP00000464121.1:p.Val365=
ENST00000581285.5:c.993C>T	ENSP00000464155.1:p.Val331=
ENST00000584828.5:c.402+44C>T
ENST00000585130.5:c.*676C>T	ENSP00000464120.1:n.*676C>T
NM_018404.2:c.1077C>T	NP_060874.1:p.Val359=
XM_005258008.2:c.1095C>T	XP_005258065.1:p.Val365=
XM_005258011.2:c.1032C>T	XP_005258068.1:p.Val344=
XM_006721973.2:c.1051+44C>T	XP_006722036.1:n.1051+44C>T
XM_011524993.1:c.1092C>T	XP_011523295.1:p.Val364=
XM_011524994.1:c.1074C>T	XP_011523296.1:p.Val358=
NM_001346712.1:c.1095C>T	NP_001333641.1:p.Val365=
NM_001346714.1:c.1074C>T	NP_001333643.1:p.Val358=
NM_001346716.1:c.1033+44C>T	NP_001333645.1:n.1033+44C>T
NR_144488.1:n.1276C>T
XM_024450831.1:c.1077C>T	XP_024306599.1:p.Val359=
XM_024450832.1:c.1092C>T	XP_024306600.1:p.Val364=
XM_024450833.1:c.1032C>T	XP_024306601.1:p.Val344=
XM_024450834.1:c.1051+44C>T	XP_024306602.1:n.1051+44C>T
XM_024450835.1:c.711C>T	XP_024306603.1:p.Val237=
NM_018404.3:c.1077C>T MANE Select	NP_060874.1:p.Val359=
NM_001346712.2:c.1095C>T	NP_001333641.1:p.Val365=
NM_001346714.2:c.1074C>T	NP_001333643.1:p.Val358=
NM_001346716.2:c.1033+44C>T	NP_001333645.1:n.1033+44C>T
NR_144488.2:n.1067C>T