Canonical Allele Identifier: CA2448298129
Gene: GLA HGNC NCBI
RPL36A-HNRNPH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101398748C= , CM000685.2:g.101398748C= GRCh38
NC_000023.10:g.100653736C= , CM000685.1:g.100653736C= GRCh37
NC_000023.9:g.100540392C= NCBI36
NG_007119.1:g.14216G= , LRG_672:g.14216G=

Transcript Alleles

HGVS Amino-acid change
ENST00000486121.7:c.*247+37G= (GLA) ENSP00000501124.2:n.*247+37G=
ENST00000674127.2:c.*304+37G= (GLA) ENSP00000501044.2:n.*304+37G=
ENST00000710365.1:c.876+37G= (GLA) ENSP00000518234.1:n.876+37G=
ENST00000218516.4:c.801+37G= (GLA) MANE Select ENSP00000218516.4:n.801+37G=
ENST00000466414.2:n.757G= (GLA)
ENST00000468823.2:n.1773G= (GLA)
ENST00000479445.2:n.1235G= (GLA)
ENST00000480513.6:c.*109+37G= (GLA) ENSP00000497055.1:n.*109+37G=
ENST00000486121.6:c.846+37G= (GLA)
ENST00000649178.1:c.924+37G= (GLA) ENSP00000498186.1:n.924+37G=
ENST00000674127.1:c.901+37G= (GLA) ENSP00000501044.1:n.901+37G=
ENST00000674142.1:n.925G= (GLA)
ENST00000674634.2:c.801+37G= (GLA) ENSP00000502629.2:n.801+37G=
ENST00000675592.1:c.801+37G= (GLA) ENSP00000502239.1:n.801+37G=
ENST00000675799.1:c.*146G= (GLA) ENSP00000502661.1:n.*146G=
ENST00000675968.1:n.3492G= (GLA)
ENST00000676156.1:c.765+37G= (GLA) ENSP00000501730.1:n.765+37G=
ENST00000676372.1:c.838G= (GLA) ENSP00000502805.1:n.838G=
ENST00000218516.3:c.801+37G= (GLA) ENSP00000218516.3:n.801+37G=
ENST00000409170.3:c.300+3291C= (RPL36A-HNRNPH2) ENSP00000386655.4:n.300+3291C=
ENST00000409338.5:c.177+6926C= (RPL36A-HNRNPH2) ENSP00000386974.2:n.177+6926C=
ENST00000468823.1:n.387G= (GLA)
ENST00000493905.6:c.*189+37G= (GLA) ENSP00000476935.1:n.*189+37G=
NM_000169.2:c.801+37G= , LRG_672t1:c.801+37G= (GLA) NP_000160.1:n.801+37G=
NM_001199973.1:c.408+3291C= (RPL36A-HNRNPH2) NP_001186902.1:n.408+3291C=
NM_001199974.1:c.285+6926C= (RPL36A-HNRNPH2) NP_001186903.1:n.285+6926C=
XR_938397.1:n.886+37G= (GLA)
XR_938397.2:n.907+37G= (GLA)
NM_001199973.2:c.300+3291C= (RPL36A-HNRNPH2) NP_001186902.2:n.300+3291C=
NM_001199974.2:c.177+6926C= (RPL36A-HNRNPH2) NP_001186903.2:n.177+6926C=
NM_000169.3:c.801+37G= (GLA) MANE Select NP_000160.1:n.801+37G=
NR_164783.1:n.880+37G= (GLA)