Canonical Allele Identifier: CA2448298824
Gene: GLA HGNC NCBI
RPL36A-HNRNPH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101400698C= , CM000685.2:g.101400698C= GRCh38
NC_000023.10:g.100655686C= , CM000685.1:g.100655686C= GRCh37
NC_000023.9:g.100542342C= NCBI36
NG_007119.1:g.12266G= , LRG_672:g.12266G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000486121.7:c.*53G= (GLA) ENSP00000501124.2:n.*53G=
ENST00000674127.2:c.*53G= (GLA) ENSP00000501044.2:n.*53G=
ENST00000710365.1:c.682G= (GLA) ENSP00000518234.1:p.Glu228=
ENST00000218516.4:c.607G= (GLA) MANE Select ENSP00000218516.4:p.Glu203=
ENST00000466414.2:n.526G= (GLA)
ENST00000468823.2:n.1542G= (GLA)
ENST00000479445.2:n.1004G= (GLA)
ENST00000480513.6:c.547+934G= (GLA) ENSP00000497055.1:n.547+934G=
ENST00000486121.6:c.652G= (GLA)
ENST00000649178.1:c.730G= (GLA) ENSP00000498186.1:p.Glu244=
ENST00000674127.1:c.650G= (GLA) ENSP00000501044.1:n.650G=
ENST00000674142.1:n.694G= (GLA)
ENST00000674634.2:c.607G= (GLA) ENSP00000502629.2:p.Glu203=
ENST00000675592.1:c.607G= (GLA) ENSP00000502239.1:p.Glu203=
ENST00000675799.1:c.547+934G= (GLA) ENSP00000502661.1:n.547+934G=
ENST00000675968.1:n.1542G= (GLA)
ENST00000676156.1:c.571G= (GLA) ENSP00000501730.1:p.Glu191=
ENST00000676372.1:c.607G= (GLA) ENSP00000502805.1:p.Glu203=
ENST00000218516.3:c.607G= (GLA) ENSP00000218516.3:p.Glu203=
ENST00000409170.3:c.300+5241C= (RPL36A-HNRNPH2) ENSP00000386655.4:n.300+5241C=
ENST00000409338.5:c.177+8876C= (RPL36A-HNRNPH2) ENSP00000386974.2:n.177+8876C=
ENST00000468823.1:n.156G= (GLA)
ENST00000480513.5:n.477+934G= (GLA)
ENST00000486121.5:n.652G= (GLA)
ENST00000493905.6:c.607G= (GLA) ENSP00000476935.1:p.Glu203=
NM_000169.2:c.607G= , LRG_672t1:c.607G= (GLA) NP_000160.1:p.Glu203=
NM_001199973.1:c.408+5241C= (RPL36A-HNRNPH2) NP_001186902.1:n.408+5241C=
NM_001199974.1:c.285+8876C= (RPL36A-HNRNPH2) NP_001186903.1:n.285+8876C=
XR_938397.1:n.635G= (GLA)
XR_938397.2:n.656G= (GLA)
NM_001199973.2:c.300+5241C= (RPL36A-HNRNPH2) NP_001186902.2:n.300+5241C=
NM_001199974.2:c.177+8876C= (RPL36A-HNRNPH2) NP_001186903.2:n.177+8876C=
NM_000169.3:c.607G= (GLA) MANE Select NP_000160.1:p.Glu203=
NR_164783.1:n.629G= (GLA)