Canonical Allele Identifier: CA775505918

Gene: GAA

Linked Data

• dbSNP Id: rs1256322599
• MyVariant Identifiers: chr17:g.78075420C>T (hg19) ; chr17:g.80101621C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.80101621C>T , CM000679.2:g.80101621C>T	GRCh38
NC_000017.10:g.78075420C>T , CM000679.1:g.78075420C>T	GRCh37
NC_000017.9:g.75690015C>T	NCBI36
NG_009822.1:g.5066C>T , LRG_673:g.5066C>T
NG_029761.1:g.69990C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000570803.6:c.-37C>T	ENSP00000460543.2:n.-37C>T
ENST00000572080.2:c.-117C>T	ENSP00000459972.2:n.-117C>T
ENST00000577106.6:c.-152C>T	ENSP00000458306.2:n.-152C>T
ENST00000302262.8:c.-302C>T MANE Select	ENSP00000305692.3:n.-302C>T
ENST00000390015.7:c.-117C>T	ENSP00000374665.3:n.-117C>T
ENST00000570803.5:c.-37C>T	ENSP00000460543.1:n.-37C>T
ENST00000574376.1:n.25C>T
ENST00000577106.5:c.-152C>T	ENSP00000458306.1:n.-152C>T
NM_000152.3:c.-302C>T , LRG_673t1:c.-302C>T	NP_000143.2:n.-302C>T
NM_001079803.1:c.-117C>T	NP_001073271.1:n.-117C>T
NM_001079804.1:c.-37C>T	NP_001073272.1:n.-37C>T
XM_005257193.1:c.-212C>T	XP_005257250.1:n.-212C>T
XM_005257194.3:c.-152C>T	XP_005257251.1:n.-152C>T
NM_000152.4:c.-302C>T	NP_000143.2:n.-302C>T
NM_001079803.2:c.-117C>T	NP_001073271.1:n.-117C>T
NM_001079804.2:c.-37C>T	NP_001073272.1:n.-37C>T
NR_134848.1:n.96C>T
XM_005257194.4:c.-152C>T	XP_005257251.1:n.-152C>T
NM_000152.5:c.-302C>T MANE Select	NP_000143.2:n.-302C>T
NM_001079803.3:c.-117C>T	NP_001073271.1:n.-117C>T
NM_001079804.3:c.-37C>T	NP_001073272.1:n.-37C>T
NR_134848.2:n.41C>T