Canonical Allele Identifier: CA2448298126
Gene: GLA HGNC NCBI
RPL36A-HNRNPH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101398741A= , CM000685.2:g.101398741A= GRCh38
NC_000023.10:g.100653729A= , CM000685.1:g.100653729A= GRCh37
NC_000023.9:g.100540385A= NCBI36
NG_007119.1:g.14223T= , LRG_672:g.14223T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000486121.7:c.*247+44T= (GLA) ENSP00000501124.2:n.*247+44T=
ENST00000674127.2:c.*304+44T= (GLA) ENSP00000501044.2:n.*304+44T=
ENST00000710365.1:c.876+44T= (GLA) ENSP00000518234.1:n.876+44T=
ENST00000218516.4:c.801+44T= (GLA) MANE Select ENSP00000218516.4:n.801+44T=
ENST00000466414.2:n.764T= (GLA)
ENST00000468823.2:n.1780T= (GLA)
ENST00000479445.2:n.1242T= (GLA)
ENST00000480513.6:c.*109+44T= (GLA) ENSP00000497055.1:n.*109+44T=
ENST00000486121.6:c.846+44T= (GLA)
ENST00000649178.1:c.924+44T= (GLA) ENSP00000498186.1:n.924+44T=
ENST00000674127.1:c.901+44T= (GLA) ENSP00000501044.1:n.901+44T=
ENST00000674142.1:n.932T= (GLA)
ENST00000674634.2:c.801+44T= (GLA) ENSP00000502629.2:n.801+44T=
ENST00000675592.1:c.801+44T= (GLA) ENSP00000502239.1:n.801+44T=
ENST00000675799.1:c.*153T= (GLA) ENSP00000502661.1:n.*153T=
ENST00000675968.1:n.3499T= (GLA)
ENST00000676156.1:c.765+44T= (GLA) ENSP00000501730.1:n.765+44T=
ENST00000676372.1:c.845T= (GLA) ENSP00000502805.1:n.845T=
ENST00000218516.3:c.801+44T= (GLA) ENSP00000218516.3:n.801+44T=
ENST00000409170.3:c.300+3284A= (RPL36A-HNRNPH2) ENSP00000386655.4:n.300+3284A=
ENST00000409338.5:c.177+6919A= (RPL36A-HNRNPH2) ENSP00000386974.2:n.177+6919A=
ENST00000468823.1:n.394T= (GLA)
ENST00000493905.6:c.*189+44T= (GLA) ENSP00000476935.1:n.*189+44T=
NM_000169.2:c.801+44T= , LRG_672t1:c.801+44T= (GLA) NP_000160.1:n.801+44T=
NM_001199973.1:c.408+3284A= (RPL36A-HNRNPH2) NP_001186902.1:n.408+3284A=
NM_001199974.1:c.285+6919A= (RPL36A-HNRNPH2) NP_001186903.1:n.285+6919A=
XR_938397.1:n.886+44T= (GLA)
XR_938397.2:n.907+44T= (GLA)
NM_001199973.2:c.300+3284A= (RPL36A-HNRNPH2) NP_001186902.2:n.300+3284A=
NM_001199974.2:c.177+6919A= (RPL36A-HNRNPH2) NP_001186903.2:n.177+6919A=
NM_000169.3:c.801+44T= (GLA) MANE Select NP_000160.1:n.801+44T=
NR_164783.1:n.880+44T= (GLA)