Canonical Allele Identifier: CA2448298810
Gene: GLA HGNC NCBI
RPL36A-HNRNPH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101400680A= , CM000685.2:g.101400680A= GRCh38
NC_000023.10:g.100655668A= , CM000685.1:g.100655668A= GRCh37
NC_000023.9:g.100542324A= NCBI36
NG_007119.1:g.12284T= , LRG_672:g.12284T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000486121.7:c.*71T= (GLA) ENSP00000501124.2:n.*71T=
ENST00000674127.2:c.*71T= (GLA) ENSP00000501044.2:n.*71T=
ENST00000710365.1:c.700T= (GLA) ENSP00000518234.1:p.Trp234=
ENST00000218516.4:c.625T= (GLA) MANE Select ENSP00000218516.4:p.Trp209=
ENST00000466414.2:n.544T= (GLA)
ENST00000468823.2:n.1560T= (GLA)
ENST00000479445.2:n.1022T= (GLA)
ENST00000480513.6:c.547+952T= (GLA) ENSP00000497055.1:n.547+952T=
ENST00000486121.6:c.670T= (GLA)
ENST00000649178.1:c.748T= (GLA) ENSP00000498186.1:p.Trp250=
ENST00000674127.1:c.668T= (GLA) ENSP00000501044.1:n.668T=
ENST00000674142.1:n.712T= (GLA)
ENST00000674634.2:c.625T= (GLA) ENSP00000502629.2:p.Trp209=
ENST00000675592.1:c.625T= (GLA) ENSP00000502239.1:p.Trp209=
ENST00000675799.1:c.547+952T= (GLA) ENSP00000502661.1:n.547+952T=
ENST00000675968.1:n.1560T= (GLA)
ENST00000676156.1:c.589T= (GLA) ENSP00000501730.1:p.Trp197=
ENST00000676372.1:c.625T= (GLA) ENSP00000502805.1:p.Trp209=
ENST00000218516.3:c.625T= (GLA) ENSP00000218516.3:p.Trp209=
ENST00000409170.3:c.300+5223A= (RPL36A-HNRNPH2) ENSP00000386655.4:n.300+5223A=
ENST00000409338.5:c.177+8858A= (RPL36A-HNRNPH2) ENSP00000386974.2:n.177+8858A=
ENST00000468823.1:n.174T= (GLA)
ENST00000480513.5:n.477+952T= (GLA)
ENST00000486121.5:n.670T= (GLA)
ENST00000493905.6:c.625T= (GLA) ENSP00000476935.1:p.Trp209=
NM_000169.2:c.625T= , LRG_672t1:c.625T= (GLA) NP_000160.1:p.Trp209=
NM_001199973.1:c.408+5223A= (RPL36A-HNRNPH2) NP_001186902.1:n.408+5223A=
NM_001199974.1:c.285+8858A= (RPL36A-HNRNPH2) NP_001186903.1:n.285+8858A=
XR_938397.1:n.653T= (GLA)
XR_938397.2:n.674T= (GLA)
NM_001199973.2:c.300+5223A= (RPL36A-HNRNPH2) NP_001186902.2:n.300+5223A=
NM_001199974.2:c.177+8858A= (RPL36A-HNRNPH2) NP_001186903.2:n.177+8858A=
NM_000169.3:c.625T= (GLA) MANE Select NP_000160.1:p.Trp209=
NR_164783.1:n.647T= (GLA)