Canonical Allele Identifier: CA1826130443
Gene: GPAA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.144084476A= , CM000670.2:g.144084476A= GRCh38
NC_000008.10:g.145139379A= , CM000670.1:g.145139379A= GRCh37
NC_000008.9:g.145211367A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000361036.11:c.697A= ENSP00000354316.6:p.Met233=
ENST00000524418.6:c.835A= ENSP00000434544.2:p.Met279=
ENST00000525087.6:c.661A= ENSP00000434485.3:p.Met221=
ENST00000525308.2:n.1272A=
ENST00000526341.6:c.*419A= ENSP00000515386.1:n.*419A=
ENST00000527144.6:c.725A= ENSP00000515403.1:p.His242=
ENST00000528073.6:c.*195A= ENSP00000435119.1:n.*195A=
ENST00000529503.6:c.*324A= ENSP00000435024.1:n.*324A=
ENST00000529638.2:n.974A=
ENST00000530258.2:n.1282A=
ENST00000530796.2:n.968A=
ENST00000531593.2:n.662A=
ENST00000532758.6:n.1484A=
ENST00000703441.1:n.978A=
ENST00000703620.1:c.871A= ENSP00000515404.1:p.Met291=
ENST00000703621.1:c.877A= ENSP00000515405.1:p.Met293=
ENST00000703622.1:c.877A= ENSP00000515406.1:p.Met293=
ENST00000703623.1:n.708A=
ENST00000703631.1:c.623A= ENSP00000515409.1:p.His208=
ENST00000703632.1:n.1056A=
ENST00000703633.1:c.835A= ENSP00000515410.1:p.Met279=
ENST00000703634.1:c.623A=
ENST00000703635.1:c.511A= ENSP00000515412.1:p.Met171=
ENST00000703647.1:n.1191A=
ENST00000703648.1:c.877A= ENSP00000515415.1:p.Met293=
ENST00000703649.1:c.877A= ENSP00000515416.1:p.Met293=
ENST00000703650.1:n.1180A=
ENST00000703651.1:n.940A=
ENST00000703652.1:n.542A=
ENST00000703653.1:n.778A=
ENST00000703654.1:n.501A=
ENST00000703670.1:n.1228A=
ENST00000703671.1:n.1269A=
ENST00000703672.1:c.*314A= ENSP00000515424.1:n.*314A=
ENST00000703673.1:n.739A=
ENST00000703674.1:n.573A=
ENST00000703675.1:n.1163A=
ENST00000703676.1:n.662A=
ENST00000703678.1:n.648A=
ENST00000703679.1:n.460A=
ENST00000703680.1:n.741A=
ENST00000703681.1:n.1235A=
ENST00000703682.1:c.386A=
ENST00000703720.1:c.*324A= ENSP00000515449.1:n.*324A=
ENST00000703721.1:n.1062A=
ENST00000703722.1:n.940A=
ENST00000703723.1:n.1328A=
ENST00000703724.1:n.99A=
ENST00000703725.1:c.877A= ENSP00000515450.1:p.Met293=
ENST00000704789.1:c.475A= ENSP00000516036.1:p.Met159=
ENST00000704790.1:n.1159A=
ENST00000704791.1:c.519A=
ENST00000704793.1:n.304A=
ENST00000704794.1:c.511A= ENSP00000516039.1:p.Met171=
ENST00000704795.1:n.821A=
ENST00000704796.1:n.860A=
ENST00000704797.1:n.1210A=
ENST00000704798.1:n.647A=
ENST00000704799.1:n.676A=
ENST00000704806.1:c.697A= ENSP00000516043.1:p.Met233=
ENST00000704807.1:c.871A= ENSP00000516044.1:p.Met291=
ENST00000704808.1:c.877A= ENSP00000516045.1:p.Met293=
ENST00000704809.1:c.835A= ENSP00000516046.1:p.Met279=
ENST00000704810.1:n.982A=
ENST00000704811.1:c.623A=
ENST00000704812.1:n.626A=
ENST00000704813.1:n.524A=
ENST00000355091.9:c.877A= MANE Select ENSP00000347206.4:p.Met293=
ENST00000355091.8:c.877A= ENSP00000347206.4:p.Met293=
ENST00000361036.10:c.697A= ENSP00000354316.6:p.Met233=
ENST00000525087.5:c.661A= ENSP00000434485.2:p.Met221=
ENST00000526233.5:n.228A=
ENST00000527144.5:n.560A=
ENST00000527653.1:n.349A=
ENST00000528073.5:c.*195A= ENSP00000435119.1:n.*195A=
ENST00000529638.1:n.204A=
ENST00000530633.1:c.*324A= ENSP00000431233.1:n.*324A=
NM_003801.3:c.877A= NP_003792.1:p.Met293=
NM_003801.4:c.877A= MANE Select NP_003792.1:p.Met293=