Canonical Allele Identifier: CA1826130446
Gene: GPAA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.144084482C= , CM000670.2:g.144084482C= GRCh38
NC_000008.10:g.145139385C= , CM000670.1:g.145139385C= GRCh37
NC_000008.9:g.145211373C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000361036.11:c.703C= ENSP00000354316.6:p.Leu235=
ENST00000524418.6:c.841C= ENSP00000434544.2:p.Leu281=
ENST00000525087.6:c.667C= ENSP00000434485.3:p.Leu223=
ENST00000525308.2:n.1278C=
ENST00000526341.6:c.*425C= ENSP00000515386.1:n.*425C=
ENST00000527144.6:c.731C= ENSP00000515403.1:p.Ser244=
ENST00000528073.6:c.*201C= ENSP00000435119.1:n.*201C=
ENST00000529503.6:c.*330C= ENSP00000435024.1:n.*330C=
ENST00000529638.2:n.980C=
ENST00000530258.2:n.1288C=
ENST00000530796.2:n.974C=
ENST00000531593.2:n.668C=
ENST00000532758.6:n.1490C=
ENST00000703441.1:n.984C=
ENST00000703620.1:c.877C= ENSP00000515404.1:p.Leu293=
ENST00000703621.1:c.883C= ENSP00000515405.1:p.Leu295=
ENST00000703622.1:c.883C= ENSP00000515406.1:p.Leu295=
ENST00000703623.1:n.714C=
ENST00000703631.1:c.629C= ENSP00000515409.1:p.Ser210=
ENST00000703632.1:n.1062C=
ENST00000703633.1:c.841C= ENSP00000515410.1:p.Leu281=
ENST00000703634.1:c.629C=
ENST00000703635.1:c.517C= ENSP00000515412.1:p.Leu173=
ENST00000703647.1:n.1197C=
ENST00000703648.1:c.883C= ENSP00000515415.1:p.Leu295=
ENST00000703649.1:c.883C= ENSP00000515416.1:p.Leu295=
ENST00000703650.1:n.1186C=
ENST00000703651.1:n.946C=
ENST00000703652.1:n.548C=
ENST00000703653.1:n.784C=
ENST00000703654.1:n.507C=
ENST00000703670.1:n.1234C=
ENST00000703671.1:n.1275C=
ENST00000703672.1:c.*320C= ENSP00000515424.1:n.*320C=
ENST00000703673.1:n.745C=
ENST00000703674.1:n.579C=
ENST00000703675.1:n.1169C=
ENST00000703676.1:n.668C=
ENST00000703678.1:n.654C=
ENST00000703679.1:n.466C=
ENST00000703680.1:n.747C=
ENST00000703681.1:n.1241C=
ENST00000703682.1:c.392C=
ENST00000703720.1:c.*330C= ENSP00000515449.1:n.*330C=
ENST00000703721.1:n.1068C=
ENST00000703722.1:n.946C=
ENST00000703723.1:n.1334C=
ENST00000703724.1:n.105C=
ENST00000703725.1:c.883C= ENSP00000515450.1:p.Leu295=
ENST00000704789.1:c.481C= ENSP00000516036.1:p.Leu161=
ENST00000704790.1:n.1165C=
ENST00000704791.1:c.525C=
ENST00000704793.1:n.310C=
ENST00000704794.1:c.517C= ENSP00000516039.1:p.Leu173=
ENST00000704795.1:n.827C=
ENST00000704796.1:n.866C=
ENST00000704797.1:n.1216C=
ENST00000704798.1:n.653C=
ENST00000704799.1:n.682C=
ENST00000704806.1:c.703C= ENSP00000516043.1:p.Leu235=
ENST00000704807.1:c.877C= ENSP00000516044.1:p.Leu293=
ENST00000704808.1:c.883C= ENSP00000516045.1:p.Leu295=
ENST00000704809.1:c.841C= ENSP00000516046.1:p.Leu281=
ENST00000704810.1:n.988C=
ENST00000704811.1:c.629C=
ENST00000704812.1:n.632C=
ENST00000704813.1:n.530C=
ENST00000355091.9:c.883C= MANE Select ENSP00000347206.4:p.Leu295=
ENST00000355091.8:c.883C= ENSP00000347206.4:p.Leu295=
ENST00000361036.10:c.703C= ENSP00000354316.6:p.Leu235=
ENST00000525087.5:c.667C= ENSP00000434485.2:p.Leu223=
ENST00000526233.5:n.234C=
ENST00000527144.5:n.566C=
ENST00000527653.1:n.355C=
ENST00000528073.5:c.*201C= ENSP00000435119.1:n.*201C=
ENST00000529638.1:n.210C=
ENST00000530633.1:c.*330C= ENSP00000431233.1:n.*330C=
NM_003801.3:c.883C= NP_003792.1:p.Leu295=
NM_003801.4:c.883C= MANE Select NP_003792.1:p.Leu295=