Canonical Allele Identifier: CA2695234981
Gene: GLA HGNC NCBI
RPL36A-HNRNPH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101401770del , CM000685.2:g.101401770del GRCh38
NC_000023.10:g.100656758del , CM000685.1:g.100656758del GRCh37
NC_000023.9:g.100543414del NCBI36
NG_007119.1:g.11194del , LRG_672:g.11194del

Transcript Alleles

HGVS Amino-acid Change
ENST00000486121.7:c.409del (GLA) ENSP00000501124.2:p.Val137LeufsTer28
ENST00000674127.2:c.409del (GLA) ENSP00000501044.2:p.Val137LeufsTer28
ENST00000710365.1:c.484del (GLA) ENSP00000518234.1:p.Val162LeufsTer28
ENST00000218516.4:c.409del (GLA) MANE Select ENSP00000218516.4:p.Val137LeufsTer28
ENST00000466414.2:n.328del (GLA)
ENST00000468823.2:n.470del (GLA)
ENST00000479445.2:n.407del (GLA)
ENST00000480513.6:c.409del (GLA) ENSP00000497055.1:p.Val137LeufsTer28
ENST00000486121.6:c.339del (GLA)
ENST00000649178.1:c.532del (GLA) ENSP00000498186.1:p.Val178LeufsTer28
ENST00000674127.1:c.337del (GLA) ENSP00000501044.1:p.Val113LeufsTer28
ENST00000674142.1:n.496del (GLA)
ENST00000674634.2:c.409del (GLA) ENSP00000502629.2:p.Val137LeufsTer28
ENST00000675592.1:c.409del (GLA) ENSP00000502239.1:p.Val137LeufsTer28
ENST00000675799.1:c.409del (GLA) ENSP00000502661.1:p.Val137LeufsTer28
ENST00000675968.1:n.470del (GLA)
ENST00000676156.1:c.409del (GLA) ENSP00000501730.1:p.Val137LeufsTer28
ENST00000676372.1:c.409del (GLA) ENSP00000502805.1:p.Val137LeufsTer28
ENST00000218516.3:c.409del (GLA) ENSP00000218516.3:p.Val137LeufsTer28
ENST00000409170.3:c.300+6313del (RPL36A-HNRNPH2) ENSP00000386655.4:n.300+6313del
ENST00000409338.5:c.177+9948del (RPL36A-HNRNPH2) ENSP00000386974.2:n.177+9948del
ENST00000479445.1:n.393del (GLA)
ENST00000480513.5:n.339del (GLA)
ENST00000486121.5:n.339del (GLA)
ENST00000493905.6:c.409del (GLA) ENSP00000476935.1:p.Val137LeufsTer28
NM_000169.2:c.409del , LRG_672t1:c.409del (GLA) NP_000160.1:p.Val137LeufsTer28
NM_001199973.1:c.408+6313del (RPL36A-HNRNPH2) NP_001186902.1:n.408+6313del
NM_001199974.1:c.285+9948del (RPL36A-HNRNPH2) NP_001186903.1:n.285+9948del
XR_938397.1:n.437del (GLA)
XR_938397.2:n.458del (GLA)
NM_001199973.2:c.300+6313del (RPL36A-HNRNPH2) NP_001186902.2:n.300+6313del
NM_001199974.2:c.177+9948del (RPL36A-HNRNPH2) NP_001186903.2:n.177+9948del
NM_000169.3:c.409del (GLA) MANE Select NP_000160.1:p.Val137LeufsTer28
NR_164783.1:n.431del (GLA)