Canonical Allele Identifier: CA913014083
Gene: GAA HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.78078831dup (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.80105032dup , CM000679.2:g.80105032dup GRCh38
NC_000017.10:g.78078831dup , CM000679.1:g.78078831dup GRCh37
NC_000017.9:g.75693426dup NCBI36
NG_009822.1:g.8477dup , LRG_673:g.8477dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000570803.6:c.446dup ENSP00000460543.2:p.Ala150GlyfsTer27
ENST00000572080.2:c.446dup ENSP00000459972.2:p.Ala150GlyfsTer27
ENST00000577106.6:c.446dup ENSP00000458306.2:p.Ala150GlyfsTer27
ENST00000302262.8:c.446dup MANE Select ENSP00000305692.3:p.Ala150GlyfsTer27
ENST00000302262.7:c.446dup ENSP00000305692.3:p.Ala150GlyfsTer27
ENST00000390015.7:c.446dup ENSP00000374665.3:p.Ala150GlyfsTer27
ENST00000570803.5:c.446dup ENSP00000460543.1:p.Ala150GlyfsTer27
ENST00000577106.5:c.446dup ENSP00000458306.1:p.Ala150GlyfsTer27
NM_000152.3:c.446dup , LRG_673t1:c.446dup NP_000143.2:p.Ala150GlyfsTer27
NM_001079803.1:c.446dup NP_001073271.1:p.Ala150GlyfsTer27
NM_001079804.1:c.446dup NP_001073272.1:p.Ala150GlyfsTer27
XM_005257193.1:c.446dup XP_005257250.1:p.Ala150GlyfsTer27
XM_005257194.3:c.446dup XP_005257251.1:p.Ala150GlyfsTer27
NM_000152.4:c.446dup NP_000143.2:p.Ala150GlyfsTer27
NM_001079803.2:c.446dup NP_001073271.1:p.Ala150GlyfsTer27
NM_001079804.2:c.446dup NP_001073272.1:p.Ala150GlyfsTer27
XM_005257193.2:c.446dup XP_005257250.1:p.Ala150GlyfsTer27
XM_005257194.4:c.446dup XP_005257251.1:p.Ala150GlyfsTer27
NM_000152.5:c.446dup MANE Select NP_000143.2:p.Ala150GlyfsTer27
NM_001079803.3:c.446dup NP_001073271.1:p.Ala150GlyfsTer27
NM_001079804.3:c.446dup NP_001073272.1:p.Ala150GlyfsTer27
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