Canonical Allele Identifier: CA2448299137
Gene: GLA HGNC NCBI
RPL36A-HNRNPH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101401674A= , CM000685.2:g.101401674A= GRCh38
NC_000023.10:g.100656662A= , CM000685.1:g.100656662A= GRCh37
NC_000023.9:g.100543318A= NCBI36
NG_007119.1:g.11290T= , LRG_672:g.11290T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000486121.7:c.505T= (GLA) ENSP00000501124.2:p.Phe169=
ENST00000674127.2:c.505T= (GLA) ENSP00000501044.2:p.Phe169=
ENST00000710365.1:c.580T= (GLA) ENSP00000518234.1:p.Phe194=
ENST00000218516.4:c.505T= (GLA) MANE Select ENSP00000218516.4:p.Phe169=
ENST00000466414.2:n.424T= (GLA)
ENST00000468823.2:n.566T= (GLA)
ENST00000479445.2:n.503T= (GLA)
ENST00000480513.6:c.505T= (GLA) ENSP00000497055.1:p.Phe169=
ENST00000486121.6:c.435T= (GLA)
ENST00000649178.1:c.628T= (GLA) ENSP00000498186.1:p.Phe210=
ENST00000674127.1:c.433T= (GLA) ENSP00000501044.1:p.Phe145=
ENST00000674142.1:n.592T= (GLA)
ENST00000674634.2:c.505T= (GLA) ENSP00000502629.2:p.Phe169=
ENST00000675592.1:c.505T= (GLA) ENSP00000502239.1:p.Phe169=
ENST00000675799.1:c.505T= (GLA) ENSP00000502661.1:p.Phe169=
ENST00000675968.1:n.566T= (GLA)
ENST00000676156.1:c.505T= (GLA) ENSP00000501730.1:p.Phe169=
ENST00000676372.1:c.505T= (GLA) ENSP00000502805.1:p.Phe169=
ENST00000218516.3:c.505T= (GLA) ENSP00000218516.3:p.Phe169=
ENST00000409170.3:c.300+6217A= (RPL36A-HNRNPH2) ENSP00000386655.4:n.300+6217A=
ENST00000409338.5:c.177+9852A= (RPL36A-HNRNPH2) ENSP00000386974.2:n.177+9852A=
ENST00000479445.1:n.489T= (GLA)
ENST00000480513.5:n.435T= (GLA)
ENST00000486121.5:n.435T= (GLA)
ENST00000493905.6:c.505T= (GLA) ENSP00000476935.1:p.Phe169=
NM_000169.2:c.505T= , LRG_672t1:c.505T= (GLA) NP_000160.1:p.Phe169=
NM_001199973.1:c.408+6217A= (RPL36A-HNRNPH2) NP_001186902.1:n.408+6217A=
NM_001199974.1:c.285+9852A= (RPL36A-HNRNPH2) NP_001186903.1:n.285+9852A=
XR_938397.1:n.533T= (GLA)
XR_938397.2:n.554T= (GLA)
NM_001199973.2:c.300+6217A= (RPL36A-HNRNPH2) NP_001186902.2:n.300+6217A=
NM_001199974.2:c.177+9852A= (RPL36A-HNRNPH2) NP_001186903.2:n.177+9852A=
NM_000169.3:c.505T= (GLA) MANE Select NP_000160.1:p.Phe169=
NR_164783.1:n.527T= (GLA)