Canonical Allele Identifier: CA1826130440
Gene: GPAA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.144084473C= , CM000670.2:g.144084473C= GRCh38
NC_000008.10:g.145139376C= , CM000670.1:g.145139376C= GRCh37
NC_000008.9:g.145211364C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000361036.11:c.694C= ENSP00000354316.6:p.Leu232=
ENST00000524418.6:c.832C= ENSP00000434544.2:p.Leu278=
ENST00000525087.6:c.658C= ENSP00000434485.3:p.Leu220=
ENST00000525308.2:n.1269C=
ENST00000526341.6:c.*416C= ENSP00000515386.1:n.*416C=
ENST00000527144.6:c.722C= ENSP00000515403.1:p.Ala241=
ENST00000528073.6:c.*192C= ENSP00000435119.1:n.*192C=
ENST00000529503.6:c.*321C= ENSP00000435024.1:n.*321C=
ENST00000529638.2:n.971C=
ENST00000530258.2:n.1279C=
ENST00000530796.2:n.965C=
ENST00000531593.2:n.659C=
ENST00000532758.6:n.1481C=
ENST00000703441.1:n.975C=
ENST00000703620.1:c.868C= ENSP00000515404.1:p.Leu290=
ENST00000703621.1:c.874C= ENSP00000515405.1:p.Leu292=
ENST00000703622.1:c.874C= ENSP00000515406.1:p.Leu292=
ENST00000703623.1:n.705C=
ENST00000703631.1:c.620C= ENSP00000515409.1:p.Ala207=
ENST00000703632.1:n.1053C=
ENST00000703633.1:c.832C= ENSP00000515410.1:p.Leu278=
ENST00000703634.1:c.620C=
ENST00000703635.1:c.508C= ENSP00000515412.1:p.Leu170=
ENST00000703647.1:n.1188C=
ENST00000703648.1:c.874C= ENSP00000515415.1:p.Leu292=
ENST00000703649.1:c.874C= ENSP00000515416.1:p.Leu292=
ENST00000703650.1:n.1177C=
ENST00000703651.1:n.937C=
ENST00000703652.1:n.539C=
ENST00000703653.1:n.775C=
ENST00000703654.1:n.498C=
ENST00000703670.1:n.1225C=
ENST00000703671.1:n.1266C=
ENST00000703672.1:c.*311C= ENSP00000515424.1:n.*311C=
ENST00000703673.1:n.736C=
ENST00000703674.1:n.570C=
ENST00000703675.1:n.1160C=
ENST00000703676.1:n.659C=
ENST00000703678.1:n.645C=
ENST00000703679.1:n.457C=
ENST00000703680.1:n.738C=
ENST00000703681.1:n.1232C=
ENST00000703682.1:c.383C=
ENST00000703720.1:c.*321C= ENSP00000515449.1:n.*321C=
ENST00000703721.1:n.1059C=
ENST00000703722.1:n.937C=
ENST00000703723.1:n.1325C=
ENST00000703724.1:n.96C=
ENST00000703725.1:c.874C= ENSP00000515450.1:p.Leu292=
ENST00000704789.1:c.472C= ENSP00000516036.1:p.Leu158=
ENST00000704790.1:n.1156C=
ENST00000704791.1:c.516C=
ENST00000704793.1:n.301C=
ENST00000704794.1:c.508C= ENSP00000516039.1:p.Leu170=
ENST00000704795.1:n.818C=
ENST00000704796.1:n.857C=
ENST00000704797.1:n.1207C=
ENST00000704798.1:n.644C=
ENST00000704799.1:n.673C=
ENST00000704806.1:c.694C= ENSP00000516043.1:p.Leu232=
ENST00000704807.1:c.868C= ENSP00000516044.1:p.Leu290=
ENST00000704808.1:c.874C= ENSP00000516045.1:p.Leu292=
ENST00000704809.1:c.832C= ENSP00000516046.1:p.Leu278=
ENST00000704810.1:n.979C=
ENST00000704811.1:c.620C=
ENST00000704812.1:n.623C=
ENST00000704813.1:n.521C=
ENST00000355091.9:c.874C= MANE Select ENSP00000347206.4:p.Leu292=
ENST00000355091.8:c.874C= ENSP00000347206.4:p.Leu292=
ENST00000361036.10:c.694C= ENSP00000354316.6:p.Leu232=
ENST00000525087.5:c.658C= ENSP00000434485.2:p.Leu220=
ENST00000526233.5:n.225C=
ENST00000527144.5:n.557C=
ENST00000527653.1:n.346C=
ENST00000528073.5:c.*192C= ENSP00000435119.1:n.*192C=
ENST00000529638.1:n.201C=
ENST00000530633.1:c.*321C= ENSP00000431233.1:n.*321C=
NM_003801.3:c.874C= NP_003792.1:p.Leu292=
NM_003801.4:c.874C= MANE Select NP_003792.1:p.Leu292=