Canonical Allele Identifier: CA2448299178
Gene: GLA HGNC NCBI
RPL36A-HNRNPH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101401753G= , CM000685.2:g.101401753G= GRCh38
NC_000023.10:g.100656741G= , CM000685.1:g.100656741G= GRCh37
NC_000023.9:g.100543397G= NCBI36
NG_007119.1:g.11211C= , LRG_672:g.11211C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000486121.7:c.426C= (GLA) ENSP00000501124.2:p.Cys142=
ENST00000674127.2:c.426C= (GLA) ENSP00000501044.2:p.Cys142=
ENST00000710365.1:c.501C= (GLA) ENSP00000518234.1:p.Cys167=
ENST00000218516.4:c.426C= (GLA) MANE Select ENSP00000218516.4:p.Cys142=
ENST00000466414.2:n.345C= (GLA)
ENST00000468823.2:n.487C= (GLA)
ENST00000479445.2:n.424C= (GLA)
ENST00000480513.6:c.426C= (GLA) ENSP00000497055.1:p.Cys142=
ENST00000486121.6:c.356C= (GLA)
ENST00000649178.1:c.549C= (GLA) ENSP00000498186.1:p.Cys183=
ENST00000674127.1:c.354C= (GLA) ENSP00000501044.1:p.Cys118=
ENST00000674142.1:n.513C= (GLA)
ENST00000674634.2:c.426C= (GLA) ENSP00000502629.2:p.Cys142=
ENST00000675592.1:c.426C= (GLA) ENSP00000502239.1:p.Cys142=
ENST00000675799.1:c.426C= (GLA) ENSP00000502661.1:p.Cys142=
ENST00000675968.1:n.487C= (GLA)
ENST00000676156.1:c.426C= (GLA) ENSP00000501730.1:p.Cys142=
ENST00000676372.1:c.426C= (GLA) ENSP00000502805.1:p.Cys142=
ENST00000218516.3:c.426C= (GLA) ENSP00000218516.3:p.Cys142=
ENST00000409170.3:c.300+6296G= (RPL36A-HNRNPH2) ENSP00000386655.4:n.300+6296G=
ENST00000409338.5:c.177+9931G= (RPL36A-HNRNPH2) ENSP00000386974.2:n.177+9931G=
ENST00000479445.1:n.410C= (GLA)
ENST00000480513.5:n.356C= (GLA)
ENST00000486121.5:n.356C= (GLA)
ENST00000493905.6:c.426C= (GLA) ENSP00000476935.1:p.Cys142=
NM_000169.2:c.426C= , LRG_672t1:c.426C= (GLA) NP_000160.1:p.Cys142=
NM_001199973.1:c.408+6296G= (RPL36A-HNRNPH2) NP_001186902.1:n.408+6296G=
NM_001199974.1:c.285+9931G= (RPL36A-HNRNPH2) NP_001186903.1:n.285+9931G=
XR_938397.1:n.454C= (GLA)
XR_938397.2:n.475C= (GLA)
NM_001199973.2:c.300+6296G= (RPL36A-HNRNPH2) NP_001186902.2:n.300+6296G=
NM_001199974.2:c.177+9931G= (RPL36A-HNRNPH2) NP_001186903.2:n.177+9931G=
NM_000169.3:c.426C= (GLA) MANE Select NP_000160.1:p.Cys142=
NR_164783.1:n.448C= (GLA)