Canonical Allele Identifier: CA398979323

Gene: ADAP2

Linked Data

• MyVariant Identifiers: chr17:g.29283390A>T (hg19) ; chr17:g.30956372A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.30956372A>T , CM000679.2:g.30956372A>T	GRCh38
NC_000017.10:g.29283390A>T , CM000679.1:g.29283390A>T	GRCh37
NC_000017.9:g.26307516A>T	NCBI36
NG_051975.1:g.39637A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330889.8:c.1014A>T MANE Select	ENSP00000329468.3:p.Arg338Ser
ENST00000330889.7:c.1014A>T	ENSP00000329468.3:p.Arg338Ser
ENST00000470962.1:n.434A>T
ENST00000480980.1:n.448A>T
ENST00000580525.5:c.1032A>T	ENSP00000464121.1:p.Arg344Ser
ENST00000581285.5:c.930A>T	ENSP00000464155.1:p.Arg310Ser
ENST00000584828.5:c.383A>T
ENST00000585130.5:c.*613A>T	ENSP00000464120.1:n.*613A>T
NM_018404.2:c.1014A>T	NP_060874.1:p.Arg338Ser
XM_005258008.2:c.1032A>T	XP_005258065.1:p.Arg344Ser
XM_005258011.2:c.969A>T	XP_005258068.1:p.Arg323Ser
XM_006721973.2:c.1032A>T	XP_006722036.1:p.Arg344Ser
XM_011524993.1:c.1029A>T	XP_011523295.1:p.Arg343Ser
XM_011524994.1:c.1011A>T	XP_011523296.1:p.Arg337Ser
NM_001346712.1:c.1032A>T	NP_001333641.1:p.Arg344Ser
NM_001346714.1:c.1011A>T	NP_001333643.1:p.Arg337Ser
NM_001346716.1:c.1014A>T	NP_001333645.1:p.Arg338Ser
NR_144488.1:n.1213A>T
XM_024450831.1:c.1014A>T	XP_024306599.1:p.Arg338Ser
XM_024450832.1:c.1029A>T	XP_024306600.1:p.Arg343Ser
XM_024450833.1:c.969A>T	XP_024306601.1:p.Arg323Ser
XM_024450834.1:c.1032A>T	XP_024306602.1:p.Arg344Ser
XM_024450835.1:c.648A>T	XP_024306603.1:p.Arg216Ser
NM_018404.3:c.1014A>T MANE Select	NP_060874.1:p.Arg338Ser
NM_001346712.2:c.1032A>T	NP_001333641.1:p.Arg344Ser
NM_001346714.2:c.1011A>T	NP_001333643.1:p.Arg337Ser
NM_001346716.2:c.1014A>T	NP_001333645.1:p.Arg338Ser
NR_144488.2:n.1004A>T