Canonical Allele Identifier: CA401361472

Gene: GAA

Linked Data

• ClinVar Variation Id: 565797
• ClinVar RCV Id: RCV000685442
• dbSNP Id: rs1567826289
• gnomAD v4: 17-80105038-C-T
• MyVariant Identifiers: chr17:g.78078837C>T (hg19) ; chr17:g.80105038C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.80105038C>T , CM000679.2:g.80105038C>T	GRCh38
NC_000017.10:g.78078837C>T , CM000679.1:g.78078837C>T	GRCh37
NC_000017.9:g.75693432C>T	NCBI36
NG_009822.1:g.8483C>T , LRG_673:g.8483C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000570803.6:c.452C>T	ENSP00000460543.2:p.Thr151Ile
ENST00000572080.2:c.452C>T	ENSP00000459972.2:p.Thr151Ile
ENST00000577106.6:c.452C>T	ENSP00000458306.2:p.Thr151Ile
ENST00000302262.8:c.452C>T MANE Select	ENSP00000305692.3:p.Thr151Ile
ENST00000302262.7:c.452C>T	ENSP00000305692.3:p.Thr151Ile
ENST00000390015.7:c.452C>T	ENSP00000374665.3:p.Thr151Ile
ENST00000570803.5:c.452C>T	ENSP00000460543.1:p.Thr151Ile
ENST00000577106.5:c.452C>T	ENSP00000458306.1:p.Thr151Ile
NM_000152.3:c.452C>T , LRG_673t1:c.452C>T	NP_000143.2:p.Thr151Ile
NM_001079803.1:c.452C>T	NP_001073271.1:p.Thr151Ile
NM_001079804.1:c.452C>T	NP_001073272.1:p.Thr151Ile
XM_005257193.1:c.452C>T	XP_005257250.1:p.Thr151Ile
XM_005257194.3:c.452C>T	XP_005257251.1:p.Thr151Ile
NM_000152.4:c.452C>T	NP_000143.2:p.Thr151Ile
NM_001079803.2:c.452C>T	NP_001073271.1:p.Thr151Ile
NM_001079804.2:c.452C>T	NP_001073272.1:p.Thr151Ile
XM_005257193.2:c.452C>T	XP_005257250.1:p.Thr151Ile
XM_005257194.4:c.452C>T	XP_005257251.1:p.Thr151Ile
NM_000152.5:c.452C>T MANE Select	NP_000143.2:p.Thr151Ile
NM_001079803.3:c.452C>T	NP_001073271.1:p.Thr151Ile
NM_001079804.3:c.452C>T	NP_001073272.1:p.Thr151Ile