Canonical Allele Identifier: CA352758
Gene: GLA HGNC NCBI
RPL36A-HNRNPH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101398082C>T , CM000685.2:g.101398082C>T GRCh38
NC_000023.10:g.100653070C>T , CM000685.1:g.100653070C>T GRCh37
NC_000023.9:g.100539726C>T NCBI36
NG_007119.1:g.14882G>A , LRG_672:g.14882G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000486121.7:c.*463G>A (GLA) ENSP00000501124.2:n.*463G>A
ENST00000674127.2:c.*520G>A (GLA) ENSP00000501044.2:n.*520G>A
ENST00000710365.1:c.1092G>A (GLA) ENSP00000518234.1:p.Val364=
ENST00000218516.4:c.1017G>A (GLA) MANE Select ENSP00000218516.4:p.Val339=
ENST00000466414.2:n.1153G>A (GLA)
ENST00000468823.2:n.2439G>A (GLA)
ENST00000479445.2:n.1631G>A (GLA)
ENST00000480513.6:c.*325G>A (GLA) ENSP00000497055.1:n.*325G>A
ENST00000486121.6:c.1062G>A (GLA)
ENST00000649178.1:c.1140G>A (GLA) ENSP00000498186.1:p.Val380=
ENST00000674127.1:c.1117G>A (GLA) ENSP00000501044.1:n.1117G>A
ENST00000674142.1:n.1321G>A (GLA)
ENST00000675592.1:c.819G>A (GLA) ENSP00000502239.1:p.Val273=
ENST00000675799.1:c.*542G>A (GLA) ENSP00000502661.1:n.*542G>A
ENST00000675968.1:n.3888G>A (GLA)
ENST00000676156.1:c.981G>A (GLA) ENSP00000501730.1:p.Val327=
ENST00000676372.1:c.1083G>A (GLA) ENSP00000502805.1:n.1083G>A
ENST00000218516.3:c.1017G>A (GLA) ENSP00000218516.3:p.Val339=
ENST00000409170.3:c.300+2625C>T (RPL36A-HNRNPH2) ENSP00000386655.4:n.300+2625C>T
ENST00000409338.5:c.177+6260C>T (RPL36A-HNRNPH2) ENSP00000386974.2:n.177+6260C>T
ENST00000466414.1:n.343G>A (GLA)
ENST00000493905.6:c.*405G>A (GLA) ENSP00000476935.1:n.*405G>A
NM_000169.2:c.1017G>A , LRG_672t1:c.1017G>A (GLA) NP_000160.1:p.Val339=
NM_001199973.1:c.408+2625C>T (RPL36A-HNRNPH2) NP_001186902.1:n.408+2625C>T
NM_001199974.1:c.285+6260C>T (RPL36A-HNRNPH2) NP_001186903.1:n.285+6260C>T
XR_938397.1:n.1102G>A (GLA)
XR_938397.2:n.1123G>A (GLA)
NM_001199973.2:c.300+2625C>T (RPL36A-HNRNPH2) NP_001186902.2:n.300+2625C>T
NM_001199974.2:c.177+6260C>T (RPL36A-HNRNPH2) NP_001186903.2:n.177+6260C>T
NM_000169.3:c.1017G>A (GLA) MANE Select NP_000160.1:p.Val339=
NR_164783.1:n.1096G>A (GLA)