Canonical Allele Identifier: CA401370488
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 2441606
ClinVar RCV Id: RCV003143444
dbSNP Id: rs1233586977

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.80113272C>T , CM000679.2:g.80113272C>T GRCh38
NC_000017.10:g.78087071C>T , CM000679.1:g.78087071C>T GRCh37
NC_000017.9:g.75701666C>T NCBI36
NG_009822.1:g.16717C>T , LRG_673:g.16717C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000570803.6:c.2095C>T ENSP00000460543.2:p.Leu699Phe
ENST00000572080.2:c.*233C>T ENSP00000459972.2:n.*233C>T
ENST00000577106.6:c.2095C>T ENSP00000458306.2:p.Leu699Phe
ENST00000302262.8:c.2095C>T MANE Select ENSP00000305692.3:p.Leu699Phe
ENST00000302262.7:c.2095C>T ENSP00000305692.3:p.Leu699Phe
ENST00000390015.7:c.2095C>T ENSP00000374665.3:p.Leu699Phe
ENST00000572080.1:c.514C>T
NM_000152.3:c.2095C>T , LRG_673t1:c.2095C>T NP_000143.2:p.Leu699Phe
NM_001079803.1:c.2095C>T NP_001073271.1:p.Leu699Phe
NM_001079804.1:c.2095C>T NP_001073272.1:p.Leu699Phe
XM_005257193.1:c.2095C>T XP_005257250.1:p.Leu699Phe
XM_005257194.3:c.2095C>T XP_005257251.1:p.Leu699Phe
NM_000152.4:c.2095C>T NP_000143.2:p.Leu699Phe
NM_001079803.2:c.2095C>T NP_001073271.1:p.Leu699Phe
NM_001079804.2:c.2095C>T NP_001073272.1:p.Leu699Phe
XM_005257193.2:c.2095C>T XP_005257250.1:p.Leu699Phe
XM_005257194.4:c.2095C>T XP_005257251.1:p.Leu699Phe
NM_000152.5:c.2095C>T MANE Select NP_000143.2:p.Leu699Phe
NM_001079803.3:c.2095C>T NP_001073271.1:p.Leu699Phe
NM_001079804.3:c.2095C>T NP_001073272.1:p.Leu699Phe