Canonical Allele Identifier: CA2448298114
Gene: GLA HGNC NCBI
RPL36A-HNRNPH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101398711G= , CM000685.2:g.101398711G= GRCh38
NC_000023.10:g.100653699G= , CM000685.1:g.100653699G= GRCh37
NC_000023.9:g.100540355G= NCBI36
NG_007119.1:g.14253C= , LRG_672:g.14253C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000486121.7:c.*247+74C= (GLA) ENSP00000501124.2:n.*247+74C=
ENST00000674127.2:c.*304+74C= (GLA) ENSP00000501044.2:n.*304+74C=
ENST00000710365.1:c.876+74C= (GLA) ENSP00000518234.1:n.876+74C=
ENST00000218516.4:c.801+74C= (GLA) MANE Select ENSP00000218516.4:n.801+74C=
ENST00000466414.2:n.794C= (GLA)
ENST00000468823.2:n.1810C= (GLA)
ENST00000479445.2:n.1272C= (GLA)
ENST00000480513.6:c.*109+74C= (GLA) ENSP00000497055.1:n.*109+74C=
ENST00000486121.6:c.846+74C= (GLA)
ENST00000649178.1:c.924+74C= (GLA) ENSP00000498186.1:n.924+74C=
ENST00000674127.1:c.901+74C= (GLA) ENSP00000501044.1:n.901+74C=
ENST00000674142.1:n.962C= (GLA)
ENST00000674634.2:c.801+74C= (GLA) ENSP00000502629.2:n.801+74C=
ENST00000675592.1:c.801+74C= (GLA) ENSP00000502239.1:n.801+74C=
ENST00000675799.1:c.*183C= (GLA) ENSP00000502661.1:n.*183C=
ENST00000675968.1:n.3529C= (GLA)
ENST00000676156.1:c.765+74C= (GLA) ENSP00000501730.1:n.765+74C=
ENST00000676372.1:c.867+8C= (GLA) ENSP00000502805.1:n.867+8C=
ENST00000218516.3:c.801+74C= (GLA) ENSP00000218516.3:n.801+74C=
ENST00000409170.3:c.300+3254G= (RPL36A-HNRNPH2) ENSP00000386655.4:n.300+3254G=
ENST00000409338.5:c.177+6889G= (RPL36A-HNRNPH2) ENSP00000386974.2:n.177+6889G=
ENST00000468823.1:n.424C= (GLA)
ENST00000493905.6:c.*189+74C= (GLA) ENSP00000476935.1:n.*189+74C=
NM_000169.2:c.801+74C= , LRG_672t1:c.801+74C= (GLA) NP_000160.1:n.801+74C=
NM_001199973.1:c.408+3254G= (RPL36A-HNRNPH2) NP_001186902.1:n.408+3254G=
NM_001199974.1:c.285+6889G= (RPL36A-HNRNPH2) NP_001186903.1:n.285+6889G=
XR_938397.1:n.886+74C= (GLA)
XR_938397.2:n.907+74C= (GLA)
NM_001199973.2:c.300+3254G= (RPL36A-HNRNPH2) NP_001186902.2:n.300+3254G=
NM_001199974.2:c.177+6889G= (RPL36A-HNRNPH2) NP_001186903.2:n.177+6889G=
NM_000169.3:c.801+74C= (GLA) MANE Select NP_000160.1:n.801+74C=
NR_164783.1:n.880+74C= (GLA)