Canonical Allele Identifier: CA2448298087
Gene: GLA HGNC NCBI
RPL36A-HNRNPH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101398618A= , CM000685.2:g.101398618A= GRCh38
NC_000023.10:g.100653606A= , CM000685.1:g.100653606A= GRCh37
NC_000023.9:g.100540262A= NCBI36
NG_007119.1:g.14346T= , LRG_672:g.14346T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000486121.7:c.*248-51T= (GLA) ENSP00000501124.2:n.*248-51T=
ENST00000674127.2:c.*305-51T= (GLA) ENSP00000501044.2:n.*305-51T=
ENST00000710365.1:c.877-51T= (GLA) ENSP00000518234.1:n.877-51T=
ENST00000218516.4:c.802-51T= (GLA) MANE Select ENSP00000218516.4:n.802-51T=
ENST00000466414.2:n.887T= (GLA)
ENST00000468823.2:n.1903T= (GLA)
ENST00000479445.2:n.1365T= (GLA)
ENST00000480513.6:c.*110-51T= (GLA) ENSP00000497055.1:n.*110-51T=
ENST00000486121.6:c.847-51T= (GLA)
ENST00000649178.1:c.925-51T= (GLA) ENSP00000498186.1:n.925-51T=
ENST00000674127.1:c.902-51T= (GLA) ENSP00000501044.1:n.902-51T=
ENST00000674142.1:n.1055T= (GLA)
ENST00000674634.2:c.802-51T= (GLA) ENSP00000502629.2:n.802-51T=
ENST00000675592.1:c.801+167T= (GLA) ENSP00000502239.1:n.801+167T=
ENST00000675799.1:c.*276T= (GLA) ENSP00000502661.1:n.*276T=
ENST00000675968.1:n.3622T= (GLA)
ENST00000676156.1:c.766-51T= (GLA) ENSP00000501730.1:n.766-51T=
ENST00000676372.1:c.868-51T= (GLA) ENSP00000502805.1:n.868-51T=
ENST00000218516.3:c.802-51T= (GLA) ENSP00000218516.3:n.802-51T=
ENST00000409170.3:c.300+3161A= (RPL36A-HNRNPH2) ENSP00000386655.4:n.300+3161A=
ENST00000409338.5:c.177+6796A= (RPL36A-HNRNPH2) ENSP00000386974.2:n.177+6796A=
ENST00000466414.1:n.77T= (GLA)
ENST00000468823.1:n.517T= (GLA)
ENST00000493905.6:c.*190-51T= (GLA) ENSP00000476935.1:n.*190-51T=
NM_000169.2:c.802-51T= , LRG_672t1:c.802-51T= (GLA) NP_000160.1:n.802-51T=
NM_001199973.1:c.408+3161A= (RPL36A-HNRNPH2) NP_001186902.1:n.408+3161A=
NM_001199974.1:c.285+6796A= (RPL36A-HNRNPH2) NP_001186903.1:n.285+6796A=
XR_938397.1:n.887-51T= (GLA)
XR_938397.2:n.908-51T= (GLA)
NM_001199973.2:c.300+3161A= (RPL36A-HNRNPH2) NP_001186902.2:n.300+3161A=
NM_001199974.2:c.177+6796A= (RPL36A-HNRNPH2) NP_001186903.2:n.177+6796A=
NM_000169.3:c.802-51T= (GLA) MANE Select NP_000160.1:n.802-51T=
NR_164783.1:n.881-51T= (GLA)