Canonical Allele Identifier: CA2695234998
Gene: GLA HGNC NCBI
RPL36A-HNRNPH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101403883_101403884del , CM000685.2:g.101403883_101403884del GRCh38
NC_000023.10:g.100658871_100658872del , CM000685.1:g.100658871_100658872del GRCh37
NC_000023.9:g.100545527_100545528del NCBI36
NG_007119.1:g.9081_9082del , LRG_672:g.9081_9082del
NG_016327.1:g.681_682del

Transcript Alleles

HGVS Amino-acid change
ENST00000486121.7:c.297_298del (GLA) ENSP00000501124.2:p.Asp101PhefsTer21
ENST00000674127.2:c.297_298del (GLA) ENSP00000501044.2:p.Asp101PhefsTer21
ENST00000710365.1:c.372_373del (GLA) ENSP00000518234.1:p.Asp126PhefsTer21
ENST00000218516.4:c.297_298del (GLA) MANE Select ENSP00000218516.4:p.Asp101PhefsTer21
ENST00000466414.2:n.216_217del (GLA)
ENST00000468823.2:n.358_359del (GLA)
ENST00000479445.2:n.295_296del (GLA)
ENST00000480513.6:c.297_298del (GLA) ENSP00000497055.1:p.Asp101PhefsTer21
ENST00000486121.6:c.227_228del (GLA)
ENST00000649178.1:c.420_421del (GLA) ENSP00000498186.1:p.Asp142PhefsTer21
ENST00000674127.1:c.225_226del (GLA) ENSP00000501044.1:p.Asp77PhefsTer21
ENST00000674142.1:n.384_385del (GLA)
ENST00000674634.2:c.297_298del (GLA) ENSP00000502629.2:p.Asp101PhefsTer21
ENST00000675592.1:c.297_298del (GLA) ENSP00000502239.1:p.Asp101PhefsTer21
ENST00000675799.1:c.297_298del (GLA) ENSP00000502661.1:p.Asp101PhefsTer21
ENST00000675968.1:n.358_359del (GLA)
ENST00000676156.1:c.297_298del (GLA) ENSP00000501730.1:p.Asp101PhefsTer21
ENST00000676372.1:c.297_298del (GLA) ENSP00000502805.1:p.Asp101PhefsTer21
ENST00000218516.3:c.297_298del (GLA) ENSP00000218516.3:p.Asp101PhefsTer21
ENST00000409170.3:c.301-8053_301-8052del (RPL36A-HNRNPH2) ENSP00000386655.4:n.301-8053_301-8052del
ENST00000409338.5:c.178-8053_178-8052del (RPL36A-HNRNPH2) ENSP00000386974.2:n.178-8053_178-8052del
ENST00000479445.1:n.281_282del (GLA)
ENST00000480513.5:n.227_228del (GLA)
ENST00000486121.5:n.227_228del (GLA)
ENST00000493905.6:c.297_298del (GLA) ENSP00000476935.1:p.Asp101PhefsTer21
NM_000169.2:c.297_298del , LRG_672t1:c.297_298del (GLA) NP_000160.1:p.Asp101PhefsTer21
NM_001199973.1:c.409-8053_409-8052del (RPL36A-HNRNPH2) NP_001186902.1:n.409-8053_409-8052del
NM_001199974.1:c.286-8053_286-8052del (RPL36A-HNRNPH2) NP_001186903.1:n.286-8053_286-8052del
XR_938397.1:n.325_326del (GLA)
XR_938397.2:n.346_347del (GLA)
NM_001199973.2:c.301-8053_301-8052del (RPL36A-HNRNPH2) NP_001186902.2:n.301-8053_301-8052del
NM_001199974.2:c.178-8053_178-8052del (RPL36A-HNRNPH2) NP_001186903.2:n.178-8053_178-8052del
NM_000169.3:c.297_298del (GLA) MANE Select NP_000160.1:p.Asp101PhefsTer21
NR_164783.1:n.319_320del (GLA)