Canonical Allele Identifier: CA2448297931
Gene: GLA HGNC NCBI
RPL36A-HNRNPH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101398326T= , CM000685.2:g.101398326T= GRCh38
NC_000023.10:g.100653314T= , CM000685.1:g.100653314T= GRCh37
NC_000023.9:g.100539970T= NCBI36
NG_007119.1:g.14638A= , LRG_672:g.14638A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000486121.7:c.*445+44A= (GLA) ENSP00000501124.2:n.*445+44A=
ENST00000674127.2:c.*502+44A= (GLA) ENSP00000501044.2:n.*502+44A=
ENST00000710365.1:c.1074+44A= (GLA) ENSP00000518234.1:n.1074+44A=
ENST00000218516.4:c.999+44A= (GLA) MANE Select ENSP00000218516.4:n.999+44A=
ENST00000466414.2:n.1135+44A= (GLA)
ENST00000468823.2:n.2195A= (GLA)
ENST00000479445.2:n.1613+44A= (GLA)
ENST00000480513.6:c.*307+44A= (GLA) ENSP00000497055.1:n.*307+44A=
ENST00000486121.6:c.1044+44A= (GLA)
ENST00000649178.1:c.1122+44A= (GLA) ENSP00000498186.1:n.1122+44A=
ENST00000674127.1:c.1099+44A= (GLA) ENSP00000501044.1:n.1099+44A=
ENST00000674142.1:n.1303+44A= (GLA)
ENST00000674634.2:c.1043A= (GLA) ENSP00000502629.2:p.Tyr348=
ENST00000675592.1:c.802-227A= (GLA) ENSP00000502239.1:n.802-227A=
ENST00000675799.1:c.*524+44A= (GLA) ENSP00000502661.1:n.*524+44A=
ENST00000675968.1:n.3870+44A= (GLA)
ENST00000676156.1:c.963+44A= (GLA) ENSP00000501730.1:n.963+44A=
ENST00000676372.1:c.1065+44A= (GLA) ENSP00000502805.1:n.1065+44A=
ENST00000218516.3:c.999+44A= (GLA) ENSP00000218516.3:n.999+44A=
ENST00000409170.3:c.300+2869T= (RPL36A-HNRNPH2) ENSP00000386655.4:n.300+2869T=
ENST00000409338.5:c.177+6504T= (RPL36A-HNRNPH2) ENSP00000386974.2:n.177+6504T=
ENST00000466414.1:n.325+44A= (GLA)
ENST00000493905.6:c.*387+44A= (GLA) ENSP00000476935.1:n.*387+44A=
NM_000169.2:c.999+44A= , LRG_672t1:c.999+44A= (GLA) NP_000160.1:n.999+44A=
NM_001199973.1:c.408+2869T= (RPL36A-HNRNPH2) NP_001186902.1:n.408+2869T=
NM_001199974.1:c.285+6504T= (RPL36A-HNRNPH2) NP_001186903.1:n.285+6504T=
XR_938397.1:n.1084+44A= (GLA)
XR_938397.2:n.1105+44A= (GLA)
NM_001199973.2:c.300+2869T= (RPL36A-HNRNPH2) NP_001186902.2:n.300+2869T=
NM_001199974.2:c.177+6504T= (RPL36A-HNRNPH2) NP_001186903.2:n.177+6504T=
NM_000169.3:c.999+44A= (GLA) MANE Select NP_000160.1:n.999+44A=
NR_164783.1:n.1078+44A= (GLA)