Canonical Allele Identifier: CA398979046
Gene: ADAP2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30956283C>A , CM000679.2:g.30956283C>A GRCh38
NC_000017.10:g.29283301C>A , CM000679.1:g.29283301C>A GRCh37
NC_000017.9:g.26307427C>A NCBI36
NG_051975.1:g.39548C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000330889.8:c.925C>A MANE Select ENSP00000329468.3:p.Gln309Lys
ENST00000330889.7:c.925C>A ENSP00000329468.3:p.Gln309Lys
ENST00000470962.1:n.345C>A
ENST00000480980.1:n.359C>A
ENST00000580525.5:c.943C>A ENSP00000464121.1:p.Gln315Lys
ENST00000581285.5:c.841C>A ENSP00000464155.1:p.Gln281Lys
ENST00000584828.5:c.294C>A
ENST00000584989.1:c.217C>A ENSP00000462634.1:p.Gln73Lys
ENST00000585130.5:c.*524C>A ENSP00000464120.1:n.*524C>A
NM_018404.2:c.925C>A NP_060874.1:p.Gln309Lys
XM_005258008.2:c.943C>A XP_005258065.1:p.Gln315Lys
XM_005258011.2:c.880C>A XP_005258068.1:p.Gln294Lys
XM_006721973.2:c.943C>A XP_006722036.1:p.Gln315Lys
XM_011524993.1:c.940C>A XP_011523295.1:p.Gln314Lys
XM_011524994.1:c.922C>A XP_011523296.1:p.Gln308Lys
NM_001346712.1:c.943C>A NP_001333641.1:p.Gln315Lys
NM_001346714.1:c.922C>A NP_001333643.1:p.Gln308Lys
NM_001346716.1:c.925C>A NP_001333645.1:p.Gln309Lys
NR_144488.1:n.1124C>A
XM_024450831.1:c.925C>A XP_024306599.1:p.Gln309Lys
XM_024450832.1:c.940C>A XP_024306600.1:p.Gln314Lys
XM_024450833.1:c.880C>A XP_024306601.1:p.Gln294Lys
XM_024450834.1:c.943C>A XP_024306602.1:p.Gln315Lys
XM_024450835.1:c.559C>A XP_024306603.1:p.Gln187Lys
NM_018404.3:c.925C>A MANE Select NP_060874.1:p.Gln309Lys
NM_001346712.2:c.943C>A NP_001333641.1:p.Gln315Lys
NM_001346714.2:c.922C>A NP_001333643.1:p.Gln308Lys
NM_001346716.2:c.925C>A NP_001333645.1:p.Gln309Lys
NR_144488.2:n.915C>A