Canonical Allele Identifier: CA2640291856
Gene: GAA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.80118883_80118884insCGGTCACCAG , CM000679.2:g.80118883_80118884insCGGTCACCAG GRCh38
NC_000017.10:g.78092682_78092683insCGGTCACCAG , CM000679.1:g.78092682_78092683insCGGTCACCAG GRCh37
NC_000017.9:g.75707277_75707278insCGGTCACCAG NCBI36
NG_009822.1:g.22328_22329insCGGTCACCAG , LRG_673:g.22328_22329insCGGTCACCAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000570803.6:c.2799+78_2799+79insCGGTCACCAG ENSP00000460543.2:n.2799+78_2799+79insCGGTCACCAG
ENST00000572080.2:c.*937+78_*937+79insCGGTCACCAG ENSP00000459972.2:n.*937+78_*937+79insCGGTCACCAG
ENST00000577106.6:c.2799+78_2799+79insCGGTCACCAG ENSP00000458306.2:n.2799+78_2799+79insCGGTCACCAG
ENST00000302262.8:c.2799+78_2799+79insCGGTCACCAG MANE Select ENSP00000305692.3:n.2799+78_2799+79insCGGTCACCAG
ENST00000302262.7:c.2799+78_2799+79insCGGTCACCAG ENSP00000305692.3:n.2799+78_2799+79insCGGTCACCAG
ENST00000390015.7:c.2799+78_2799+79insCGGTCACCAG ENSP00000374665.3:n.2799+78_2799+79insCGGTCACCAG
ENST00000573556.1:n.752+78_752+79insCGGTCACCAG
NM_000152.3:c.2799+78_2799+79insCGGTCACCAG , LRG_673t1:c.2799+78_2799+79insCGGTCACCAG NP_000143.2:n.2799+78_2799+79insCGGTCACCAG
NM_001079803.1:c.2799+78_2799+79insCGGTCACCAG NP_001073271.1:n.2799+78_2799+79insCGGTCACCAG
NM_001079804.1:c.2799+78_2799+79insCGGTCACCAG NP_001073272.1:n.2799+78_2799+79insCGGTCACCAG
XM_005257193.1:c.2799+78_2799+79insCGGTCACCAG XP_005257250.1:n.2799+78_2799+79insCGGTCACCAG
XM_005257194.3:c.2799+78_2799+79insCGGTCACCAG XP_005257251.1:n.2799+78_2799+79insCGGTCACCAG
NM_000152.4:c.2799+78_2799+79insCGGTCACCAG NP_000143.2:n.2799+78_2799+79insCGGTCACCAG
NM_001079803.2:c.2799+78_2799+79insCGGTCACCAG NP_001073271.1:n.2799+78_2799+79insCGGTCACCAG
NM_001079804.2:c.2799+78_2799+79insCGGTCACCAG NP_001073272.1:n.2799+78_2799+79insCGGTCACCAG
XM_005257193.2:c.2799+78_2799+79insCGGTCACCAG XP_005257250.1:n.2799+78_2799+79insCGGTCACCAG
XM_005257194.4:c.2799+78_2799+79insCGGTCACCAG XP_005257251.1:n.2799+78_2799+79insCGGTCACCAG
NM_000152.5:c.2799+78_2799+79insCGGTCACCAG MANE Select NP_000143.2:n.2799+78_2799+79insCGGTCACCAG
NM_001079803.3:c.2799+78_2799+79insCGGTCACCAG NP_001073271.1:n.2799+78_2799+79insCGGTCACCAG
NM_001079804.3:c.2799+78_2799+79insCGGTCACCAG NP_001073272.1:n.2799+78_2799+79insCGGTCACCAG