Canonical Allele Identifier: CA2448297869
Gene: GLA HGNC NCBI
RPL36A-HNRNPH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101398121G= , CM000685.2:g.101398121G= GRCh38
NC_000023.10:g.100653109G= , CM000685.1:g.100653109G= GRCh37
NC_000023.9:g.100539765G= NCBI36
NG_007119.1:g.14843C= , LRG_672:g.14843C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000486121.7:c.*446-22C= (GLA) ENSP00000501124.2:n.*446-22C=
ENST00000674127.2:c.*503-22C= (GLA) ENSP00000501044.2:n.*503-22C=
ENST00000710365.1:c.1075-22C= (GLA) ENSP00000518234.1:n.1075-22C=
ENST00000218516.4:c.1000-22C= (GLA) MANE Select ENSP00000218516.4:n.1000-22C=
ENST00000466414.2:n.1136-22C= (GLA)
ENST00000468823.2:n.2400C= (GLA)
ENST00000479445.2:n.1614-22C= (GLA)
ENST00000480513.6:c.*308-22C= (GLA) ENSP00000497055.1:n.*308-22C=
ENST00000486121.6:c.1045-22C= (GLA)
ENST00000649178.1:c.1123-22C= (GLA) ENSP00000498186.1:n.1123-22C=
ENST00000674127.1:c.1100-22C= (GLA) ENSP00000501044.1:n.1100-22C=
ENST00000674142.1:n.1304-22C= (GLA)
ENST00000675592.1:c.802-22C= (GLA) ENSP00000502239.1:n.802-22C=
ENST00000675799.1:c.*525-22C= (GLA) ENSP00000502661.1:n.*525-22C=
ENST00000675968.1:n.3871-22C= (GLA)
ENST00000676156.1:c.964-22C= (GLA) ENSP00000501730.1:n.964-22C=
ENST00000676372.1:c.1066-22C= (GLA) ENSP00000502805.1:n.1066-22C=
ENST00000218516.3:c.1000-22C= (GLA) ENSP00000218516.3:n.1000-22C=
ENST00000409170.3:c.300+2664G= (RPL36A-HNRNPH2) ENSP00000386655.4:n.300+2664G=
ENST00000409338.5:c.177+6299G= (RPL36A-HNRNPH2) ENSP00000386974.2:n.177+6299G=
ENST00000466414.1:n.326-22C= (GLA)
ENST00000493905.6:c.*388-22C= (GLA) ENSP00000476935.1:n.*388-22C=
NM_000169.2:c.1000-22C= , LRG_672t1:c.1000-22C= (GLA) NP_000160.1:n.1000-22C=
NM_001199973.1:c.408+2664G= (RPL36A-HNRNPH2) NP_001186902.1:n.408+2664G=
NM_001199974.1:c.285+6299G= (RPL36A-HNRNPH2) NP_001186903.1:n.285+6299G=
XR_938397.1:n.1085-22C= (GLA)
XR_938397.2:n.1106-22C= (GLA)
NM_001199973.2:c.300+2664G= (RPL36A-HNRNPH2) NP_001186902.2:n.300+2664G=
NM_001199974.2:c.177+6299G= (RPL36A-HNRNPH2) NP_001186903.2:n.177+6299G=
NM_000169.3:c.1000-22C= (GLA) MANE Select NP_000160.1:n.1000-22C=
NR_164783.1:n.1079-22C= (GLA)