Canonical Allele Identifier: CA2448298822
Gene: GLA HGNC NCBI
RPL36A-HNRNPH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101400694C= , CM000685.2:g.101400694C= GRCh38
NC_000023.10:g.100655682C= , CM000685.1:g.100655682C= GRCh37
NC_000023.9:g.100542338C= NCBI36
NG_007119.1:g.12270G= , LRG_672:g.12270G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000486121.7:c.*57G= (GLA) ENSP00000501124.2:n.*57G=
ENST00000674127.2:c.*57G= (GLA) ENSP00000501044.2:n.*57G=
ENST00000710365.1:c.686G= (GLA) ENSP00000518234.1:p.Trp229=
ENST00000218516.4:c.611G= (GLA) MANE Select ENSP00000218516.4:p.Trp204=
ENST00000466414.2:n.530G= (GLA)
ENST00000468823.2:n.1546G= (GLA)
ENST00000479445.2:n.1008G= (GLA)
ENST00000480513.6:c.547+938G= (GLA) ENSP00000497055.1:n.547+938G=
ENST00000486121.6:c.656G= (GLA)
ENST00000649178.1:c.734G= (GLA) ENSP00000498186.1:p.Trp245=
ENST00000674127.1:c.654G= (GLA) ENSP00000501044.1:n.654G=
ENST00000674142.1:n.698G= (GLA)
ENST00000674634.2:c.611G= (GLA) ENSP00000502629.2:p.Trp204=
ENST00000675592.1:c.611G= (GLA) ENSP00000502239.1:p.Trp204=
ENST00000675799.1:c.547+938G= (GLA) ENSP00000502661.1:n.547+938G=
ENST00000675968.1:n.1546G= (GLA)
ENST00000676156.1:c.575G= (GLA) ENSP00000501730.1:p.Trp192=
ENST00000676372.1:c.611G= (GLA) ENSP00000502805.1:p.Trp204=
ENST00000218516.3:c.611G= (GLA) ENSP00000218516.3:p.Trp204=
ENST00000409170.3:c.300+5237C= (RPL36A-HNRNPH2) ENSP00000386655.4:n.300+5237C=
ENST00000409338.5:c.177+8872C= (RPL36A-HNRNPH2) ENSP00000386974.2:n.177+8872C=
ENST00000468823.1:n.160G= (GLA)
ENST00000480513.5:n.477+938G= (GLA)
ENST00000486121.5:n.656G= (GLA)
ENST00000493905.6:c.611G= (GLA) ENSP00000476935.1:p.Trp204=
NM_000169.2:c.611G= , LRG_672t1:c.611G= (GLA) NP_000160.1:p.Trp204=
NM_001199973.1:c.408+5237C= (RPL36A-HNRNPH2) NP_001186902.1:n.408+5237C=
NM_001199974.1:c.285+8872C= (RPL36A-HNRNPH2) NP_001186903.1:n.285+8872C=
XR_938397.1:n.639G= (GLA)
XR_938397.2:n.660G= (GLA)
NM_001199973.2:c.300+5237C= (RPL36A-HNRNPH2) NP_001186902.2:n.300+5237C=
NM_001199974.2:c.177+8872C= (RPL36A-HNRNPH2) NP_001186903.2:n.177+8872C=
NM_000169.3:c.611G= (GLA) MANE Select NP_000160.1:p.Trp204=
NR_164783.1:n.633G= (GLA)