Canonical Allele Identifier: CA2695235000
Gene: GLA HGNC NCBI
RPL36A-HNRNPH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101403894_101403899delinsA , CM000685.2:g.101403894_101403899delinsA GRCh38
NC_000023.10:g.100658882_100658887delinsA , CM000685.1:g.100658882_100658887delinsA GRCh37
NC_000023.9:g.100545538_100545543delinsA NCBI36
NG_007119.1:g.9065_9070delinsT , LRG_672:g.9065_9070delinsT
NG_016327.1:g.692_697delinsA

Transcript Alleles

HGVS Amino-acid change
ENST00000486121.7:c.281_286delinsT (GLA) ENSP00000501124.2:p.Cys94PhefsTer27
ENST00000674127.2:c.281_286delinsT (GLA) ENSP00000501044.2:p.Cys94PhefsTer27
ENST00000710365.1:c.356_361delinsT (GLA) ENSP00000518234.1:p.Cys119PhefsTer27
ENST00000218516.4:c.281_286delinsT (GLA) MANE Select ENSP00000218516.4:p.Cys94PhefsTer27
ENST00000466414.2:n.200_205delinsT (GLA)
ENST00000468823.2:n.342_347delinsT (GLA)
ENST00000479445.2:n.279_284delinsT (GLA)
ENST00000480513.6:c.281_286delinsT (GLA) ENSP00000497055.1:p.Cys94PhefsTer27
ENST00000486121.6:c.211_216delinsT (GLA)
ENST00000649178.1:c.404_409delinsT (GLA) ENSP00000498186.1:p.Cys135PhefsTer27
ENST00000674127.1:c.209_214delinsT (GLA) ENSP00000501044.1:p.Cys70PhefsTer27
ENST00000674142.1:n.368_373delinsT (GLA)
ENST00000674634.2:c.281_286delinsT (GLA) ENSP00000502629.2:p.Cys94PhefsTer27
ENST00000675592.1:c.281_286delinsT (GLA) ENSP00000502239.1:p.Cys94PhefsTer27
ENST00000675799.1:c.281_286delinsT (GLA) ENSP00000502661.1:p.Cys94PhefsTer27
ENST00000675968.1:n.342_347delinsT (GLA)
ENST00000676156.1:c.281_286delinsT (GLA) ENSP00000501730.1:p.Cys94PhefsTer27
ENST00000676372.1:c.281_286delinsT (GLA) ENSP00000502805.1:p.Cys94PhefsTer27
ENST00000218516.3:c.281_286delinsT (GLA) ENSP00000218516.3:p.Cys94PhefsTer27
ENST00000409170.3:c.301-8042_301-8037delinsA (RPL36A-HNRNPH2) ENSP00000386655.4:n.301-8042_301-8037deli...
ENST00000409338.5:c.178-8042_178-8037delinsA (RPL36A-HNRNPH2) ENSP00000386974.2:n.178-8042_178-8037deli...
ENST00000479445.1:n.265_270delinsT (GLA)
ENST00000480513.5:n.211_216delinsT (GLA)
ENST00000486121.5:n.211_216delinsT (GLA)
ENST00000493905.6:c.281_286delinsT (GLA) ENSP00000476935.1:p.Cys94PhefsTer27
NM_000169.2:c.281_286delinsT , LRG_672t1:c.281_286delinsT (GLA) NP_000160.1:p.Cys94PhefsTer27
NM_001199973.1:c.409-8042_409-8037delinsA (RPL36A-HNRNPH2) NP_001186902.1:n.409-8042_409-8037delinsA...
NM_001199974.1:c.286-8042_286-8037delinsA (RPL36A-HNRNPH2) NP_001186903.1:n.286-8042_286-8037delinsA...
XR_938397.1:n.309_314delinsT (GLA)
XR_938397.2:n.330_335delinsT (GLA)
NM_001199973.2:c.301-8042_301-8037delinsA (RPL36A-HNRNPH2) NP_001186902.2:n.301-8042_301-8037delinsA...
NM_001199974.2:c.178-8042_178-8037delinsA (RPL36A-HNRNPH2) NP_001186903.2:n.178-8042_178-8037delinsA...
NM_000169.3:c.281_286delinsT (GLA) MANE Select NP_000160.1:p.Cys94PhefsTer27
NR_164783.1:n.303_308delinsT (GLA)