Canonical Allele Identifier: CA401370282
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 834913
ClinVar RCV Id: RCV001035696
dbSNP Id: rs2039286160

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.80113218C>T , CM000679.2:g.80113218C>T GRCh38
NC_000017.10:g.78087017C>T , CM000679.1:g.78087017C>T GRCh37
NC_000017.9:g.75701612C>T NCBI36
NG_009822.1:g.16663C>T , LRG_673:g.16663C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000570803.6:c.2041C>T ENSP00000460543.2:p.Pro681Ser
ENST00000572080.2:c.*179C>T ENSP00000459972.2:n.*179C>T
ENST00000577106.6:c.2041C>T ENSP00000458306.2:p.Pro681Ser
ENST00000302262.8:c.2041C>T MANE Select ENSP00000305692.3:p.Pro681Ser
ENST00000302262.7:c.2041C>T ENSP00000305692.3:p.Pro681Ser
ENST00000390015.7:c.2041C>T ENSP00000374665.3:p.Pro681Ser
ENST00000570716.1:n.481C>T
ENST00000572080.1:c.460C>T
NM_000152.3:c.2041C>T , LRG_673t1:c.2041C>T NP_000143.2:p.Pro681Ser
NM_001079803.1:c.2041C>T NP_001073271.1:p.Pro681Ser
NM_001079804.1:c.2041C>T NP_001073272.1:p.Pro681Ser
XM_005257193.1:c.2041C>T XP_005257250.1:p.Pro681Ser
XM_005257194.3:c.2041C>T XP_005257251.1:p.Pro681Ser
NM_000152.4:c.2041C>T NP_000143.2:p.Pro681Ser
NM_001079803.2:c.2041C>T NP_001073271.1:p.Pro681Ser
NM_001079804.2:c.2041C>T NP_001073272.1:p.Pro681Ser
XM_005257193.2:c.2041C>T XP_005257250.1:p.Pro681Ser
XM_005257194.4:c.2041C>T XP_005257251.1:p.Pro681Ser
NM_000152.5:c.2041C>T MANE Select NP_000143.2:p.Pro681Ser
NM_001079803.3:c.2041C>T NP_001073271.1:p.Pro681Ser
NM_001079804.3:c.2041C>T NP_001073272.1:p.Pro681Ser