Canonical Allele Identifier: CA499226537

Gene: ADAP2

Linked Data

• MyVariant Identifiers: chr17:g.29283393T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.30956375T>C , CM000679.2:g.30956375T>C	GRCh38
NC_000017.10:g.29283393T>C , CM000679.1:g.29283393T>C	GRCh37
NC_000017.9:g.26307519T>C	NCBI36
NG_051975.1:g.39640T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330889.8:c.1017T>C MANE Select	ENSP00000329468.3:p.Phe339=
ENST00000330889.7:c.1017T>C	ENSP00000329468.3:p.Phe339=
ENST00000470962.1:n.437T>C
ENST00000480980.1:n.451T>C
ENST00000580525.5:c.1035T>C	ENSP00000464121.1:p.Phe345=
ENST00000581285.5:c.933T>C	ENSP00000464155.1:p.Phe311=
ENST00000584828.5:c.386T>C
ENST00000585130.5:c.*616T>C	ENSP00000464120.1:n.*616T>C
NM_018404.2:c.1017T>C	NP_060874.1:p.Phe339=
XM_005258008.2:c.1035T>C	XP_005258065.1:p.Phe345=
XM_005258011.2:c.972T>C	XP_005258068.1:p.Phe324=
XM_006721973.2:c.1035T>C	XP_006722036.1:p.Phe345=
XM_011524993.1:c.1032T>C	XP_011523295.1:p.Phe344=
XM_011524994.1:c.1014T>C	XP_011523296.1:p.Phe338=
NM_001346712.1:c.1035T>C	NP_001333641.1:p.Phe345=
NM_001346714.1:c.1014T>C	NP_001333643.1:p.Phe338=
NM_001346716.1:c.1017T>C	NP_001333645.1:p.Phe339=
NR_144488.1:n.1216T>C
XM_024450831.1:c.1017T>C	XP_024306599.1:p.Phe339=
XM_024450832.1:c.1032T>C	XP_024306600.1:p.Phe344=
XM_024450833.1:c.972T>C	XP_024306601.1:p.Phe324=
XM_024450834.1:c.1035T>C	XP_024306602.1:p.Phe345=
XM_024450835.1:c.651T>C	XP_024306603.1:p.Phe217=
NM_018404.3:c.1017T>C MANE Select	NP_060874.1:p.Phe339=
NM_001346712.2:c.1035T>C	NP_001333641.1:p.Phe345=
NM_001346714.2:c.1014T>C	NP_001333643.1:p.Phe338=
NM_001346716.2:c.1017T>C	NP_001333645.1:p.Phe339=
NR_144488.2:n.1007T>C