Canonical Allele Identifier: CA413920432
Gene: GLA HGNC NCBI
RPL36A-HNRNPH2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101397973C>A , CM000685.2:g.101397973C>A GRCh38
NC_000023.10:g.100652961C>A , CM000685.1:g.100652961C>A GRCh37
NC_000023.9:g.100539617C>A NCBI36
NG_007119.1:g.14991G>T , LRG_672:g.14991G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000486121.7:c.*572G>T (GLA) ENSP00000501124.2:n.*572G>T
ENST00000674127.2:c.*629G>T (GLA) ENSP00000501044.2:n.*629G>T
ENST00000710365.1:c.1201G>T (GLA) ENSP00000518234.1:p.Val401Leu
ENST00000218516.4:c.1126G>T (GLA) MANE Select ENSP00000218516.4:p.Val376Leu
ENST00000466414.2:n.1262G>T (GLA)
ENST00000468823.2:n.2548G>T (GLA)
ENST00000479445.2:n.1740G>T (GLA)
ENST00000480513.6:c.*434G>T (GLA) ENSP00000497055.1:n.*434G>T
ENST00000486121.6:c.1171G>T (GLA)
ENST00000649178.1:c.1249G>T (GLA) ENSP00000498186.1:p.Val417Leu
ENST00000674127.1:c.1226G>T (GLA) ENSP00000501044.1:n.1226G>T
ENST00000674142.1:n.1421+9G>T (GLA)
ENST00000675592.1:c.928G>T (GLA) ENSP00000502239.1:p.Val310Leu
ENST00000675799.1:c.*651G>T (GLA) ENSP00000502661.1:n.*651G>T
ENST00000675968.1:n.3997G>T (GLA)
ENST00000676156.1:c.1090G>T (GLA) ENSP00000501730.1:p.Val364Leu
ENST00000676372.1:c.1192G>T (GLA) ENSP00000502805.1:n.1192G>T
ENST00000218516.3:c.1126G>T (GLA) ENSP00000218516.3:p.Val376Leu
ENST00000409170.3:c.300+2516C>A (RPL36A-HNRNPH2) ENSP00000386655.4:n.300+2516C>A
ENST00000409338.5:c.177+6151C>A (RPL36A-HNRNPH2) ENSP00000386974.2:n.177+6151C>A
ENST00000466414.1:n.452G>T (GLA)
ENST00000493905.6:c.*514G>T (GLA) ENSP00000476935.1:n.*514G>T
NM_000169.2:c.1126G>T , LRG_672t1:c.1126G>T (GLA) NP_000160.1:p.Val376Leu
NM_001199973.1:c.408+2516C>A (RPL36A-HNRNPH2) NP_001186902.1:n.408+2516C>A
NM_001199974.1:c.285+6151C>A (RPL36A-HNRNPH2) NP_001186903.1:n.285+6151C>A
XR_938397.1:n.1211G>T (GLA)
XR_938397.2:n.1232G>T (GLA)
NM_001199973.2:c.300+2516C>A (RPL36A-HNRNPH2) NP_001186902.2:n.300+2516C>A
NM_001199974.2:c.177+6151C>A (RPL36A-HNRNPH2) NP_001186903.2:n.177+6151C>A
NM_000169.3:c.1126G>T (GLA) MANE Select NP_000160.1:p.Val376Leu
NR_164783.1:n.1205G>T (GLA)