Canonical Allele Identifier: CA2448298061
Gene: GLA HGNC NCBI
RPL36A-HNRNPH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101398557C= , CM000685.2:g.101398557C= GRCh38
NC_000023.10:g.100653545C= , CM000685.1:g.100653545C= GRCh37
NC_000023.9:g.100540201C= NCBI36
NG_007119.1:g.14407G= , LRG_672:g.14407G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000486121.7:c.*258G= (GLA) ENSP00000501124.2:n.*258G=
ENST00000674127.2:c.*315G= (GLA) ENSP00000501044.2:n.*315G=
ENST00000710365.1:c.887G= (GLA) ENSP00000518234.1:p.Gly296=
ENST00000218516.4:c.812G= (GLA) MANE Select ENSP00000218516.4:p.Gly271=
ENST00000466414.2:n.948G= (GLA)
ENST00000468823.2:n.1964G= (GLA)
ENST00000479445.2:n.1426G= (GLA)
ENST00000480513.6:c.*120G= (GLA) ENSP00000497055.1:n.*120G=
ENST00000486121.6:c.857G= (GLA)
ENST00000649178.1:c.935G= (GLA) ENSP00000498186.1:p.Gly312=
ENST00000674127.1:c.912G= (GLA) ENSP00000501044.1:n.912G=
ENST00000674142.1:n.1116G= (GLA)
ENST00000674634.2:c.812G= (GLA) ENSP00000502629.2:p.Gly271=
ENST00000675592.1:c.801+228G= (GLA) ENSP00000502239.1:n.801+228G=
ENST00000675799.1:c.*337G= (GLA) ENSP00000502661.1:n.*337G=
ENST00000675968.1:n.3683G= (GLA)
ENST00000676156.1:c.776G= (GLA) ENSP00000501730.1:p.Gly259=
ENST00000676372.1:c.878G= (GLA) ENSP00000502805.1:n.878G=
ENST00000218516.3:c.812G= (GLA) ENSP00000218516.3:p.Gly271=
ENST00000409170.3:c.300+3100C= (RPL36A-HNRNPH2) ENSP00000386655.4:n.300+3100C=
ENST00000409338.5:c.177+6735C= (RPL36A-HNRNPH2) ENSP00000386974.2:n.177+6735C=
ENST00000466414.1:n.138G= (GLA)
ENST00000468823.1:n.578G= (GLA)
ENST00000493905.6:c.*200G= (GLA) ENSP00000476935.1:n.*200G=
NM_000169.2:c.812G= , LRG_672t1:c.812G= (GLA) NP_000160.1:p.Gly271=
NM_001199973.1:c.408+3100C= (RPL36A-HNRNPH2) NP_001186902.1:n.408+3100C=
NM_001199974.1:c.285+6735C= (RPL36A-HNRNPH2) NP_001186903.1:n.285+6735C=
XR_938397.1:n.897G= (GLA)
XR_938397.2:n.918G= (GLA)
NM_001199973.2:c.300+3100C= (RPL36A-HNRNPH2) NP_001186902.2:n.300+3100C=
NM_001199974.2:c.177+6735C= (RPL36A-HNRNPH2) NP_001186903.2:n.177+6735C=
NM_000169.3:c.812G= (GLA) MANE Select NP_000160.1:p.Gly271=
NR_164783.1:n.891G= (GLA)