Canonical Allele Identifier: CA2448297972
Gene: GLA HGNC NCBI
RPL36A-HNRNPH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101398402G= , CM000685.2:g.101398402G= GRCh38
NC_000023.10:g.100653390G= , CM000685.1:g.100653390G= GRCh37
NC_000023.9:g.100540046G= NCBI36
NG_007119.1:g.14562C= , LRG_672:g.14562C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000486121.7:c.*413C= (GLA) ENSP00000501124.2:n.*413C=
ENST00000674127.2:c.*470C= (GLA) ENSP00000501044.2:n.*470C=
ENST00000710365.1:c.1042C= (GLA) ENSP00000518234.1:p.Pro348=
ENST00000218516.4:c.967C= (GLA) MANE Select ENSP00000218516.4:p.Pro323=
ENST00000466414.2:n.1103C= (GLA)
ENST00000468823.2:n.2119C= (GLA)
ENST00000479445.2:n.1581C= (GLA)
ENST00000480513.6:c.*275C= (GLA) ENSP00000497055.1:n.*275C=
ENST00000486121.6:c.1012C= (GLA)
ENST00000649178.1:c.1090C= (GLA) ENSP00000498186.1:p.Pro364=
ENST00000674127.1:c.1067C= (GLA) ENSP00000501044.1:n.1067C=
ENST00000674142.1:n.1271C= (GLA)
ENST00000674634.2:c.967C= (GLA) ENSP00000502629.2:p.Pro323=
ENST00000675592.1:c.802-303C= (GLA) ENSP00000502239.1:n.802-303C=
ENST00000675799.1:c.*492C= (GLA) ENSP00000502661.1:n.*492C=
ENST00000675968.1:n.3838C= (GLA)
ENST00000676156.1:c.931C= (GLA) ENSP00000501730.1:p.Pro311=
ENST00000676372.1:c.1033C= (GLA) ENSP00000502805.1:n.1033C=
ENST00000218516.3:c.967C= (GLA) ENSP00000218516.3:p.Pro323=
ENST00000409170.3:c.300+2945G= (RPL36A-HNRNPH2) ENSP00000386655.4:n.300+2945G=
ENST00000409338.5:c.177+6580G= (RPL36A-HNRNPH2) ENSP00000386974.2:n.177+6580G=
ENST00000466414.1:n.293C= (GLA)
ENST00000493905.6:c.*355C= (GLA) ENSP00000476935.1:n.*355C=
NM_000169.2:c.967C= , LRG_672t1:c.967C= (GLA) NP_000160.1:p.Pro323=
NM_001199973.1:c.408+2945G= (RPL36A-HNRNPH2) NP_001186902.1:n.408+2945G=
NM_001199974.1:c.285+6580G= (RPL36A-HNRNPH2) NP_001186903.1:n.285+6580G=
XR_938397.1:n.1052C= (GLA)
XR_938397.2:n.1073C= (GLA)
NM_001199973.2:c.300+2945G= (RPL36A-HNRNPH2) NP_001186902.2:n.300+2945G=
NM_001199974.2:c.177+6580G= (RPL36A-HNRNPH2) NP_001186903.2:n.177+6580G=
NM_000169.3:c.967C= (GLA) MANE Select NP_000160.1:p.Pro323=
NR_164783.1:n.1046C= (GLA)