Canonical Allele Identifier: CA2277812531
Gene: GAA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.80108059_80108082delinsGCTCCTAAGGAGGGTTCTGGGGCC , CM000679.2:g.80108059_80108082delinsGCTCCTAAGGAGGGTTCTGGGGCC GRCh38
NC_000017.10:g.78081858_78081881delinsGCTCCTAAGGAGGGTTCTGGGGCC , CM000679.1:g.78081858_78081881delinsGCTCCTAAGGAGGGTTCTGGGGCC GRCh37
NC_000017.9:g.75696453_75696476delinsGCTCCTAAGGAGGGTTCTGGGGCC NCBI36
NG_009822.1:g.11504_11527delinsGCTCCTAAGGAGGGTTCTGGGGCC , LRG_673:g.11504_11527delinsGCTCCTAAGGAGGGTTCTGGGGCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000570803.6:c.955+163_955+186delinsGCTCCTAAGGAGGGTTCTGGGGCC ENSP00000460543.2:n.955+163_955+186delinsGCTCCTAAGGAGGGTTCTGG...
ENST00000572080.2:c.955+163_955+186delinsGCTCCTAAGGAGGGTTCTGGGGCC ENSP00000459972.2:n.955+163_955+186delinsGCTCCTAAGGAGGGTTCTGG...
ENST00000577106.6:c.955+163_955+186delinsGCTCCTAAGGAGGGTTCTGGGGCC ENSP00000458306.2:n.955+163_955+186delinsGCTCCTAAGGAGGGTTCTGG...
ENST00000302262.8:c.955+163_955+186delinsGCTCCTAAGGAGGGTTCTGGGGCC MANE Select ENSP00000305692.3:n.955+163_955+186delinsGCTCCTAAGGAGGGTTCTGG...
ENST00000302262.7:c.955+163_955+186delinsGCTCCTAAGGAGGGTTCTGGGGCC ENSP00000305692.3:n.955+163_955+186delinsGCTCCTAAGGAGGGTTCTGG...
ENST00000390015.7:c.955+163_955+186delinsGCTCCTAAGGAGGGTTCTGGGGCC ENSP00000374665.3:n.955+163_955+186delinsGCTCCTAAGGAGGGTTCTGG...
NM_000152.3:c.955+163_955+186delinsGCTCCTAAGGAGGGTTCTGGGGCC , LRG_673t1:c.955+163_955+186delinsGCTCCTAAGGAGGGTTCTGGGGCC NP_000143.2:n.955+163_955+186delinsGCTCCTAAGGAGGGTTCTGGGGCC
NM_001079803.1:c.955+163_955+186delinsGCTCCTAAGGAGGGTTCTGGGGCC NP_001073271.1:n.955+163_955+186delinsGCTCCTAAGGAGGGTTCTGGGGC...
NM_001079804.1:c.955+163_955+186delinsGCTCCTAAGGAGGGTTCTGGGGCC NP_001073272.1:n.955+163_955+186delinsGCTCCTAAGGAGGGTTCTGGGGC...
XM_005257193.1:c.955+163_955+186delinsGCTCCTAAGGAGGGTTCTGGGGCC XP_005257250.1:n.955+163_955+186delinsGCTCCTAAGGAGGGTTCTGGGGC...
XM_005257194.3:c.955+163_955+186delinsGCTCCTAAGGAGGGTTCTGGGGCC XP_005257251.1:n.955+163_955+186delinsGCTCCTAAGGAGGGTTCTGGGGC...
NM_000152.4:c.955+163_955+186delinsGCTCCTAAGGAGGGTTCTGGGGCC NP_000143.2:n.955+163_955+186delinsGCTCCTAAGGAGGGTTCTGGGGCC
NM_001079803.2:c.955+163_955+186delinsGCTCCTAAGGAGGGTTCTGGGGCC NP_001073271.1:n.955+163_955+186delinsGCTCCTAAGGAGGGTTCTGGGGC...
NM_001079804.2:c.955+163_955+186delinsGCTCCTAAGGAGGGTTCTGGGGCC NP_001073272.1:n.955+163_955+186delinsGCTCCTAAGGAGGGTTCTGGGGC...
XM_005257193.2:c.955+163_955+186delinsGCTCCTAAGGAGGGTTCTGGGGCC XP_005257250.1:n.955+163_955+186delinsGCTCCTAAGGAGGGTTCTGGGGC...
XM_005257194.4:c.955+163_955+186delinsGCTCCTAAGGAGGGTTCTGGGGCC XP_005257251.1:n.955+163_955+186delinsGCTCCTAAGGAGGGTTCTGGGGC...
NM_000152.5:c.955+163_955+186delinsGCTCCTAAGGAGGGTTCTGGGGCC MANE Select NP_000143.2:n.955+163_955+186delinsGCTCCTAAGGAGGGTTCTGGGGCC
NM_001079803.3:c.955+163_955+186delinsGCTCCTAAGGAGGGTTCTGGGGCC NP_001073271.1:n.955+163_955+186delinsGCTCCTAAGGAGGGTTCTGGGGC...
NM_001079804.3:c.955+163_955+186delinsGCTCCTAAGGAGGGTTCTGGGGCC NP_001073272.1:n.955+163_955+186delinsGCTCCTAAGGAGGGTTCTGGGGC...