Canonical Allele Identifier: CA2448298130
Gene: GLA HGNC NCBI
RPL36A-HNRNPH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101398749C= , CM000685.2:g.101398749C= GRCh38
NC_000023.10:g.100653737C= , CM000685.1:g.100653737C= GRCh37
NC_000023.9:g.100540393C= NCBI36
NG_007119.1:g.14215G= , LRG_672:g.14215G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000486121.7:c.*247+36G= (GLA) ENSP00000501124.2:n.*247+36G=
ENST00000674127.2:c.*304+36G= (GLA) ENSP00000501044.2:n.*304+36G=
ENST00000710365.1:c.876+36G= (GLA) ENSP00000518234.1:n.876+36G=
ENST00000218516.4:c.801+36G= (GLA) MANE Select ENSP00000218516.4:n.801+36G=
ENST00000466414.2:n.756G= (GLA)
ENST00000468823.2:n.1772G= (GLA)
ENST00000479445.2:n.1234G= (GLA)
ENST00000480513.6:c.*109+36G= (GLA) ENSP00000497055.1:n.*109+36G=
ENST00000486121.6:c.846+36G= (GLA)
ENST00000649178.1:c.924+36G= (GLA) ENSP00000498186.1:n.924+36G=
ENST00000674127.1:c.901+36G= (GLA) ENSP00000501044.1:n.901+36G=
ENST00000674142.1:n.924G= (GLA)
ENST00000674634.2:c.801+36G= (GLA) ENSP00000502629.2:n.801+36G=
ENST00000675592.1:c.801+36G= (GLA) ENSP00000502239.1:n.801+36G=
ENST00000675799.1:c.*145G= (GLA) ENSP00000502661.1:n.*145G=
ENST00000675968.1:n.3491G= (GLA)
ENST00000676156.1:c.765+36G= (GLA) ENSP00000501730.1:n.765+36G=
ENST00000676372.1:c.837G= (GLA) ENSP00000502805.1:n.837G=
ENST00000218516.3:c.801+36G= (GLA) ENSP00000218516.3:n.801+36G=
ENST00000409170.3:c.300+3292C= (RPL36A-HNRNPH2) ENSP00000386655.4:n.300+3292C=
ENST00000409338.5:c.177+6927C= (RPL36A-HNRNPH2) ENSP00000386974.2:n.177+6927C=
ENST00000468823.1:n.386G= (GLA)
ENST00000493905.6:c.*189+36G= (GLA) ENSP00000476935.1:n.*189+36G=
NM_000169.2:c.801+36G= , LRG_672t1:c.801+36G= (GLA) NP_000160.1:n.801+36G=
NM_001199973.1:c.408+3292C= (RPL36A-HNRNPH2) NP_001186902.1:n.408+3292C=
NM_001199974.1:c.285+6927C= (RPL36A-HNRNPH2) NP_001186903.1:n.285+6927C=
XR_938397.1:n.886+36G= (GLA)
XR_938397.2:n.907+36G= (GLA)
NM_001199973.2:c.300+3292C= (RPL36A-HNRNPH2) NP_001186902.2:n.300+3292C=
NM_001199974.2:c.177+6927C= (RPL36A-HNRNPH2) NP_001186903.2:n.177+6927C=
NM_000169.3:c.801+36G= (GLA) MANE Select NP_000160.1:n.801+36G=
NR_164783.1:n.880+36G= (GLA)