Canonical Allele Identifier: CA16602209
Gene: GLA HGNC NCBI
RPL36A-HNRNPH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101398080del , CM000685.2:g.101398080del GRCh38
NC_000023.10:g.100653068del , CM000685.1:g.100653068del GRCh37
NC_000023.9:g.100539724del NCBI36
NG_007119.1:g.14886del , LRG_672:g.14886del

Transcript Alleles

HGVS Amino-acid change
ENST00000486121.7:c.*467del (GLA) ENSP00000501124.2:n.*467del
ENST00000674127.2:c.*524del (GLA) ENSP00000501044.2:n.*524del
ENST00000710365.1:c.1096del (GLA) ENSP00000518234.1:p.Glu366AsnfsTer7
ENST00000218516.4:c.1021del (GLA) MANE Select ENSP00000218516.4:p.Glu341AsnfsTer7
ENST00000466414.2:n.1157del (GLA)
ENST00000468823.2:n.2443del (GLA)
ENST00000479445.2:n.1635del (GLA)
ENST00000480513.6:c.*329del (GLA) ENSP00000497055.1:n.*329del
ENST00000486121.6:c.1066del (GLA)
ENST00000649178.1:c.1144del (GLA) ENSP00000498186.1:p.Glu382AsnfsTer7
ENST00000674127.1:c.1121del (GLA) ENSP00000501044.1:n.1121del
ENST00000674142.1:n.1325del (GLA)
ENST00000675592.1:c.823del (GLA) ENSP00000502239.1:p.Glu275AsnfsTer7
ENST00000675799.1:c.*546del (GLA) ENSP00000502661.1:n.*546del
ENST00000675968.1:n.3892del (GLA)
ENST00000676156.1:c.985del (GLA) ENSP00000501730.1:p.Glu329AsnfsTer7
ENST00000676372.1:c.1087del (GLA) ENSP00000502805.1:n.1087del
ENST00000218516.3:c.1021del (GLA) ENSP00000218516.3:p.Glu341AsnfsTer7
ENST00000409170.3:c.300+2623del (RPL36A-HNRNPH2) ENSP00000386655.4:n.300+2623del
ENST00000409338.5:c.177+6258del (RPL36A-HNRNPH2) ENSP00000386974.2:n.177+6258del
ENST00000466414.1:n.347del (GLA)
ENST00000493905.6:c.*409del (GLA) ENSP00000476935.1:n.*409del
NM_000169.2:c.1021del , LRG_672t1:c.1021del (GLA) NP_000160.1:p.Glu341AsnfsTer7
NM_001199973.1:c.408+2623del (RPL36A-HNRNPH2) NP_001186902.1:n.408+2623del
NM_001199974.1:c.285+6258del (RPL36A-HNRNPH2) NP_001186903.1:n.285+6258del
XR_938397.1:n.1106del (GLA)
XR_938397.2:n.1127del (GLA)
NM_001199973.2:c.300+2623del (RPL36A-HNRNPH2) NP_001186902.2:n.300+2623del
NM_001199974.2:c.177+6258del (RPL36A-HNRNPH2) NP_001186903.2:n.177+6258del
NM_000169.3:c.1021del (GLA) MANE Select NP_000160.1:p.Glu341AsnfsTer7
NR_164783.1:n.1100del (GLA)