Canonical Allele Identifier: CA499226476

Gene: ADAP2

Linked Data

• MyVariant Identifiers: chr17:g.29283381A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.30956363A>T , CM000679.2:g.30956363A>T	GRCh38
NC_000017.10:g.29283381A>T , CM000679.1:g.29283381A>T	GRCh37
NC_000017.9:g.26307507A>T	NCBI36
NG_051975.1:g.39628A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330889.8:c.1005A>T MANE Select	ENSP00000329468.3:p.Pro335=
ENST00000330889.7:c.1005A>T	ENSP00000329468.3:p.Pro335=
ENST00000470962.1:n.425A>T
ENST00000480980.1:n.439A>T
ENST00000580525.5:c.1023A>T	ENSP00000464121.1:p.Pro341=
ENST00000581285.5:c.921A>T	ENSP00000464155.1:p.Pro307=
ENST00000584828.5:c.374A>T
ENST00000585130.5:c.*604A>T	ENSP00000464120.1:n.*604A>T
NM_018404.2:c.1005A>T	NP_060874.1:p.Pro335=
XM_005258008.2:c.1023A>T	XP_005258065.1:p.Pro341=
XM_005258011.2:c.960A>T	XP_005258068.1:p.Pro320=
XM_006721973.2:c.1023A>T	XP_006722036.1:p.Pro341=
XM_011524993.1:c.1020A>T	XP_011523295.1:p.Pro340=
XM_011524994.1:c.1002A>T	XP_011523296.1:p.Pro334=
NM_001346712.1:c.1023A>T	NP_001333641.1:p.Pro341=
NM_001346714.1:c.1002A>T	NP_001333643.1:p.Pro334=
NM_001346716.1:c.1005A>T	NP_001333645.1:p.Pro335=
NR_144488.1:n.1204A>T
XM_024450831.1:c.1005A>T	XP_024306599.1:p.Pro335=
XM_024450832.1:c.1020A>T	XP_024306600.1:p.Pro340=
XM_024450833.1:c.960A>T	XP_024306601.1:p.Pro320=
XM_024450834.1:c.1023A>T	XP_024306602.1:p.Pro341=
XM_024450835.1:c.639A>T	XP_024306603.1:p.Pro213=
NM_018404.3:c.1005A>T MANE Select	NP_060874.1:p.Pro335=
NM_001346712.2:c.1023A>T	NP_001333641.1:p.Pro341=
NM_001346714.2:c.1002A>T	NP_001333643.1:p.Pro334=
NM_001346716.2:c.1005A>T	NP_001333645.1:p.Pro335=
NR_144488.2:n.995A>T