Canonical Allele Identifier: CA401327063
Gene: GAA HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.78092536A>C (hg19) chr17:g.80118737A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.80118737A>C , CM000679.2:g.80118737A>C GRCh38
NC_000017.10:g.78092536A>C , CM000679.1:g.78092536A>C GRCh37
NC_000017.9:g.75707131A>C NCBI36
NG_009822.1:g.22182A>C , LRG_673:g.22182A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000570803.6:c.2731A>C ENSP00000460543.2:p.Thr911Pro
ENST00000572080.2:c.*869A>C ENSP00000459972.2:n.*869A>C
ENST00000577106.6:c.2731A>C ENSP00000458306.2:p.Thr911Pro
ENST00000302262.8:c.2731A>C MANE Select ENSP00000305692.3:p.Thr911Pro
ENST00000302262.7:c.2731A>C ENSP00000305692.3:p.Thr911Pro
ENST00000390015.7:c.2731A>C ENSP00000374665.3:p.Thr911Pro
ENST00000573556.1:n.684A>C
NM_000152.3:c.2731A>C , LRG_673t1:c.2731A>C NP_000143.2:p.Thr911Pro
NM_001079803.1:c.2731A>C NP_001073271.1:p.Thr911Pro
NM_001079804.1:c.2731A>C NP_001073272.1:p.Thr911Pro
XM_005257193.1:c.2731A>C XP_005257250.1:p.Thr911Pro
XM_005257194.3:c.2731A>C XP_005257251.1:p.Thr911Pro
NM_000152.4:c.2731A>C NP_000143.2:p.Thr911Pro
NM_001079803.2:c.2731A>C NP_001073271.1:p.Thr911Pro
NM_001079804.2:c.2731A>C NP_001073272.1:p.Thr911Pro
XM_005257193.2:c.2731A>C XP_005257250.1:p.Thr911Pro
XM_005257194.4:c.2731A>C XP_005257251.1:p.Thr911Pro
NM_000152.5:c.2731A>C MANE Select NP_000143.2:p.Thr911Pro
NM_001079803.3:c.2731A>C NP_001073271.1:p.Thr911Pro
NM_001079804.3:c.2731A>C NP_001073272.1:p.Thr911Pro
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