Canonical Allele Identifier: CA2448299154
Gene: GLA HGNC NCBI
RPL36A-HNRNPH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101401706G= , CM000685.2:g.101401706G= GRCh38
NC_000023.10:g.100656694G= , CM000685.1:g.100656694G= GRCh37
NC_000023.9:g.100543350G= NCBI36
NG_007119.1:g.11258C= , LRG_672:g.11258C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000486121.7:c.473C= (GLA) ENSP00000501124.2:p.Thr158=
ENST00000674127.2:c.473C= (GLA) ENSP00000501044.2:p.Thr158=
ENST00000710365.1:c.548C= (GLA) ENSP00000518234.1:p.Thr183=
ENST00000218516.4:c.473C= (GLA) MANE Select ENSP00000218516.4:p.Thr158=
ENST00000466414.2:n.392C= (GLA)
ENST00000468823.2:n.534C= (GLA)
ENST00000479445.2:n.471C= (GLA)
ENST00000480513.6:c.473C= (GLA) ENSP00000497055.1:p.Thr158=
ENST00000486121.6:c.403C= (GLA)
ENST00000649178.1:c.596C= (GLA) ENSP00000498186.1:p.Thr199=
ENST00000674127.1:c.401C= (GLA) ENSP00000501044.1:p.Thr134=
ENST00000674142.1:n.560C= (GLA)
ENST00000674634.2:c.473C= (GLA) ENSP00000502629.2:p.Thr158=
ENST00000675592.1:c.473C= (GLA) ENSP00000502239.1:p.Thr158=
ENST00000675799.1:c.473C= (GLA) ENSP00000502661.1:p.Thr158=
ENST00000675968.1:n.534C= (GLA)
ENST00000676156.1:c.473C= (GLA) ENSP00000501730.1:p.Thr158=
ENST00000676372.1:c.473C= (GLA) ENSP00000502805.1:p.Thr158=
ENST00000218516.3:c.473C= (GLA) ENSP00000218516.3:p.Thr158=
ENST00000409170.3:c.300+6249G= (RPL36A-HNRNPH2) ENSP00000386655.4:n.300+6249G=
ENST00000409338.5:c.177+9884G= (RPL36A-HNRNPH2) ENSP00000386974.2:n.177+9884G=
ENST00000479445.1:n.457C= (GLA)
ENST00000480513.5:n.403C= (GLA)
ENST00000486121.5:n.403C= (GLA)
ENST00000493905.6:c.473C= (GLA) ENSP00000476935.1:p.Thr158=
NM_000169.2:c.473C= , LRG_672t1:c.473C= (GLA) NP_000160.1:p.Thr158=
NM_001199973.1:c.408+6249G= (RPL36A-HNRNPH2) NP_001186902.1:n.408+6249G=
NM_001199974.1:c.285+9884G= (RPL36A-HNRNPH2) NP_001186903.1:n.285+9884G=
XR_938397.1:n.501C= (GLA)
XR_938397.2:n.522C= (GLA)
NM_001199973.2:c.300+6249G= (RPL36A-HNRNPH2) NP_001186902.2:n.300+6249G=
NM_001199974.2:c.177+9884G= (RPL36A-HNRNPH2) NP_001186903.2:n.177+9884G=
NM_000169.3:c.473C= (GLA) MANE Select NP_000160.1:p.Thr158=
NR_164783.1:n.495C= (GLA)