Canonical Allele Identifier: CA2448297926
Gene: GLA HGNC NCBI
RPL36A-HNRNPH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101398301A= , CM000685.2:g.101398301A= GRCh38
NC_000023.10:g.100653289A= , CM000685.1:g.100653289A= GRCh37
NC_000023.9:g.100539945A= NCBI36
NG_007119.1:g.14663T= , LRG_672:g.14663T=

Transcript Alleles

HGVS Amino-acid change
ENST00000486121.7:c.*445+69T= (GLA) ENSP00000501124.2:n.*445+69T=
ENST00000674127.2:c.*502+69T= (GLA) ENSP00000501044.2:n.*502+69T=
ENST00000710365.1:c.1074+69T= (GLA) ENSP00000518234.1:n.1074+69T=
ENST00000218516.4:c.999+69T= (GLA) MANE Select ENSP00000218516.4:n.999+69T=
ENST00000466414.2:n.1135+69T= (GLA)
ENST00000468823.2:n.2220T= (GLA)
ENST00000479445.2:n.1613+69T= (GLA)
ENST00000480513.6:c.*307+69T= (GLA) ENSP00000497055.1:n.*307+69T=
ENST00000486121.6:c.1044+69T= (GLA)
ENST00000649178.1:c.1122+69T= (GLA) ENSP00000498186.1:n.1122+69T=
ENST00000674127.1:c.1099+69T= (GLA) ENSP00000501044.1:n.1099+69T=
ENST00000674142.1:n.1303+69T= (GLA)
ENST00000674634.2:c.1068T= (GLA) ENSP00000502629.2:p.Ser356=
ENST00000675592.1:c.802-202T= (GLA) ENSP00000502239.1:n.802-202T=
ENST00000675799.1:c.*524+69T= (GLA) ENSP00000502661.1:n.*524+69T=
ENST00000675968.1:n.3870+69T= (GLA)
ENST00000676156.1:c.963+69T= (GLA) ENSP00000501730.1:n.963+69T=
ENST00000676372.1:c.1065+69T= (GLA) ENSP00000502805.1:n.1065+69T=
ENST00000218516.3:c.999+69T= (GLA) ENSP00000218516.3:n.999+69T=
ENST00000409170.3:c.300+2844A= (RPL36A-HNRNPH2) ENSP00000386655.4:n.300+2844A=
ENST00000409338.5:c.177+6479A= (RPL36A-HNRNPH2) ENSP00000386974.2:n.177+6479A=
ENST00000466414.1:n.325+69T= (GLA)
ENST00000493905.6:c.*387+69T= (GLA) ENSP00000476935.1:n.*387+69T=
NM_000169.2:c.999+69T= , LRG_672t1:c.999+69T= (GLA) NP_000160.1:n.999+69T=
NM_001199973.1:c.408+2844A= (RPL36A-HNRNPH2) NP_001186902.1:n.408+2844A=
NM_001199974.1:c.285+6479A= (RPL36A-HNRNPH2) NP_001186903.1:n.285+6479A=
XR_938397.1:n.1084+69T= (GLA)
XR_938397.2:n.1105+69T= (GLA)
NM_001199973.2:c.300+2844A= (RPL36A-HNRNPH2) NP_001186902.2:n.300+2844A=
NM_001199974.2:c.177+6479A= (RPL36A-HNRNPH2) NP_001186903.2:n.177+6479A=
NM_000169.3:c.999+69T= (GLA) MANE Select NP_000160.1:n.999+69T=
NR_164783.1:n.1078+69T= (GLA)