Canonical Allele Identifier: CA413920107
Gene: GLA HGNC NCBI
RPL36A-HNRNPH2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101397943G>C , CM000685.2:g.101397943G>C GRCh38
NC_000023.10:g.100652931G>C , CM000685.1:g.100652931G>C GRCh37
NC_000023.9:g.100539587G>C NCBI36
NG_007119.1:g.15021C>G , LRG_672:g.15021C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000486121.7:c.*602C>G (GLA) ENSP00000501124.2:n.*602C>G
ENST00000674127.2:c.*659C>G (GLA) ENSP00000501044.2:n.*659C>G
ENST00000710365.1:c.1231C>G (GLA) ENSP00000518234.1:p.Gln411Glu
ENST00000218516.4:c.1156C>G (GLA) MANE Select ENSP00000218516.4:p.Gln386Glu
ENST00000466414.2:n.1292C>G (GLA)
ENST00000468823.2:n.2578C>G (GLA)
ENST00000479445.2:n.1770C>G (GLA)
ENST00000480513.6:c.*464C>G (GLA) ENSP00000497055.1:n.*464C>G
ENST00000486121.6:c.1201C>G (GLA)
ENST00000649178.1:c.1279C>G (GLA) ENSP00000498186.1:p.Gln427Glu
ENST00000674127.1:c.1256C>G (GLA) ENSP00000501044.1:n.1256C>G
ENST00000674142.1:n.1421+39C>G (GLA)
ENST00000675592.1:c.958C>G (GLA) ENSP00000502239.1:p.Gln320Glu
ENST00000675799.1:c.*681C>G (GLA) ENSP00000502661.1:n.*681C>G
ENST00000675968.1:n.4027C>G (GLA)
ENST00000676156.1:c.1120C>G (GLA) ENSP00000501730.1:p.Gln374Glu
ENST00000676372.1:c.1222C>G (GLA) ENSP00000502805.1:n.1222C>G
ENST00000218516.3:c.1156C>G (GLA) ENSP00000218516.3:p.Gln386Glu
ENST00000409170.3:c.300+2486G>C (RPL36A-HNRNPH2) ENSP00000386655.4:n.300+2486G>C
ENST00000409338.5:c.177+6121G>C (RPL36A-HNRNPH2) ENSP00000386974.2:n.177+6121G>C
ENST00000466414.1:n.482C>G (GLA)
ENST00000493905.6:c.*544C>G (GLA) ENSP00000476935.1:n.*544C>G
NM_000169.2:c.1156C>G , LRG_672t1:c.1156C>G (GLA) NP_000160.1:p.Gln386Glu
NM_001199973.1:c.408+2486G>C (RPL36A-HNRNPH2) NP_001186902.1:n.408+2486G>C
NM_001199974.1:c.285+6121G>C (RPL36A-HNRNPH2) NP_001186903.1:n.285+6121G>C
XR_938397.1:n.1241C>G (GLA)
XR_938397.2:n.1262C>G (GLA)
NM_001199973.2:c.300+2486G>C (RPL36A-HNRNPH2) NP_001186902.2:n.300+2486G>C
NM_001199974.2:c.177+6121G>C (RPL36A-HNRNPH2) NP_001186903.2:n.177+6121G>C
NM_000169.3:c.1156C>G (GLA) MANE Select NP_000160.1:p.Gln386Glu
NR_164783.1:n.1235C>G (GLA)