Canonical Allele Identifier: CA2277818164
Gene: GAA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.80118689_80118694delinsGAGGGA , CM000679.2:g.80118689_80118694delinsGAGGGA GRCh38
NC_000017.10:g.78092488_78092493delinsGAGGGA , CM000679.1:g.78092488_78092493delinsGAGGGA GRCh37
NC_000017.9:g.75707083_75707088delinsGAGGGA NCBI36
NG_009822.1:g.22134_22139delinsGAGGGA , LRG_673:g.22134_22139delinsGAGGGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000570803.6:c.2683_2688delinsGAGGGA ENSP00000460543.2:p.Glu895=
ENST00000572080.2:c.*821_*826delinsGAGGGA ENSP00000459972.2:n.*821_*826delinsGAGGGA
ENST00000577106.6:c.2683_2688delinsGAGGGA ENSP00000458306.2:p.Glu895=
ENST00000302262.8:c.2683_2688delinsGAGGGA MANE Select ENSP00000305692.3:p.Glu895=
ENST00000302262.7:c.2683_2688delinsGAGGGA ENSP00000305692.3:p.Glu895=
ENST00000390015.7:c.2683_2688delinsGAGGGA ENSP00000374665.3:p.Glu895=
ENST00000573556.1:n.636_641delinsGAGGGA
NM_000152.3:c.2683_2688delinsGAGGGA , LRG_673t1:c.2683_2688delinsGAGGGA NP_000143.2:p.Glu895=
NM_001079803.1:c.2683_2688delinsGAGGGA NP_001073271.1:p.Glu895=
NM_001079804.1:c.2683_2688delinsGAGGGA NP_001073272.1:p.Glu895=
XM_005257193.1:c.2683_2688delinsGAGGGA XP_005257250.1:p.Glu895=
XM_005257194.3:c.2683_2688delinsGAGGGA XP_005257251.1:p.Glu895=
NM_000152.4:c.2683_2688delinsGAGGGA NP_000143.2:p.Glu895=
NM_001079803.2:c.2683_2688delinsGAGGGA NP_001073271.1:p.Glu895=
NM_001079804.2:c.2683_2688delinsGAGGGA NP_001073272.1:p.Glu895=
XM_005257193.2:c.2683_2688delinsGAGGGA XP_005257250.1:p.Glu895=
XM_005257194.4:c.2683_2688delinsGAGGGA XP_005257251.1:p.Glu895=
NM_000152.5:c.2683_2688delinsGAGGGA MANE Select NP_000143.2:p.Glu895=
NM_001079803.3:c.2683_2688delinsGAGGGA NP_001073271.1:p.Glu895=
NM_001079804.3:c.2683_2688delinsGAGGGA NP_001073272.1:p.Glu895=