Canonical Allele Identifier: CA2448298128
Gene: GLA HGNC NCBI
RPL36A-HNRNPH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101398743G= , CM000685.2:g.101398743G= GRCh38
NC_000023.10:g.100653731G= , CM000685.1:g.100653731G= GRCh37
NC_000023.9:g.100540387G= NCBI36
NG_007119.1:g.14221C= , LRG_672:g.14221C=

Transcript Alleles

HGVS Amino-acid change
ENST00000486121.7:c.*247+42C= (GLA) ENSP00000501124.2:n.*247+42C=
ENST00000674127.2:c.*304+42C= (GLA) ENSP00000501044.2:n.*304+42C=
ENST00000710365.1:c.876+42C= (GLA) ENSP00000518234.1:n.876+42C=
ENST00000218516.4:c.801+42C= (GLA) MANE Select ENSP00000218516.4:n.801+42C=
ENST00000466414.2:n.762C= (GLA)
ENST00000468823.2:n.1778C= (GLA)
ENST00000479445.2:n.1240C= (GLA)
ENST00000480513.6:c.*109+42C= (GLA) ENSP00000497055.1:n.*109+42C=
ENST00000486121.6:c.846+42C= (GLA)
ENST00000649178.1:c.924+42C= (GLA) ENSP00000498186.1:n.924+42C=
ENST00000674127.1:c.901+42C= (GLA) ENSP00000501044.1:n.901+42C=
ENST00000674142.1:n.930C= (GLA)
ENST00000674634.2:c.801+42C= (GLA) ENSP00000502629.2:n.801+42C=
ENST00000675592.1:c.801+42C= (GLA) ENSP00000502239.1:n.801+42C=
ENST00000675799.1:c.*151C= (GLA) ENSP00000502661.1:n.*151C=
ENST00000675968.1:n.3497C= (GLA)
ENST00000676156.1:c.765+42C= (GLA) ENSP00000501730.1:n.765+42C=
ENST00000676372.1:c.843C= (GLA) ENSP00000502805.1:n.843C=
ENST00000218516.3:c.801+42C= (GLA) ENSP00000218516.3:n.801+42C=
ENST00000409170.3:c.300+3286G= (RPL36A-HNRNPH2) ENSP00000386655.4:n.300+3286G=
ENST00000409338.5:c.177+6921G= (RPL36A-HNRNPH2) ENSP00000386974.2:n.177+6921G=
ENST00000468823.1:n.392C= (GLA)
ENST00000493905.6:c.*189+42C= (GLA) ENSP00000476935.1:n.*189+42C=
NM_000169.2:c.801+42C= , LRG_672t1:c.801+42C= (GLA) NP_000160.1:n.801+42C=
NM_001199973.1:c.408+3286G= (RPL36A-HNRNPH2) NP_001186902.1:n.408+3286G=
NM_001199974.1:c.285+6921G= (RPL36A-HNRNPH2) NP_001186903.1:n.285+6921G=
XR_938397.1:n.886+42C= (GLA)
XR_938397.2:n.907+42C= (GLA)
NM_001199973.2:c.300+3286G= (RPL36A-HNRNPH2) NP_001186902.2:n.300+3286G=
NM_001199974.2:c.177+6921G= (RPL36A-HNRNPH2) NP_001186903.2:n.177+6921G=
NM_000169.3:c.801+42C= (GLA) MANE Select NP_000160.1:n.801+42C=
NR_164783.1:n.880+42C= (GLA)