Canonical Allele Identifier: CA413921088
Gene: GLA HGNC NCBI
RPL36A-HNRNPH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101398053C>T , CM000685.2:g.101398053C>T GRCh38
NC_000023.10:g.100653041C>T , CM000685.1:g.100653041C>T GRCh37
NC_000023.9:g.100539697C>T NCBI36
NG_007119.1:g.14911G>A , LRG_672:g.14911G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000486121.7:c.*492G>A (GLA) ENSP00000501124.2:n.*492G>A
ENST00000674127.2:c.*549G>A (GLA) ENSP00000501044.2:n.*549G>A
ENST00000710365.1:c.1121G>A (GLA) ENSP00000518234.1:p.Trp374Ter
ENST00000218516.4:c.1046G>A (GLA) MANE Select ENSP00000218516.4:p.Trp349Ter
ENST00000466414.2:n.1182G>A (GLA)
ENST00000468823.2:n.2468G>A (GLA)
ENST00000479445.2:n.1660G>A (GLA)
ENST00000480513.6:c.*354G>A (GLA) ENSP00000497055.1:n.*354G>A
ENST00000486121.6:c.1091G>A (GLA)
ENST00000649178.1:c.1169G>A (GLA) ENSP00000498186.1:p.Trp390Ter
ENST00000674127.1:c.1146G>A (GLA) ENSP00000501044.1:n.1146G>A
ENST00000674142.1:n.1350G>A (GLA)
ENST00000675592.1:c.848G>A (GLA) ENSP00000502239.1:p.Trp283Ter
ENST00000675799.1:c.*571G>A (GLA) ENSP00000502661.1:n.*571G>A
ENST00000675968.1:n.3917G>A (GLA)
ENST00000676156.1:c.1010G>A (GLA) ENSP00000501730.1:p.Trp337Ter
ENST00000676372.1:c.1112G>A (GLA) ENSP00000502805.1:n.1112G>A
ENST00000218516.3:c.1046G>A (GLA) ENSP00000218516.3:p.Trp349Ter
ENST00000409170.3:c.300+2596C>T (RPL36A-HNRNPH2) ENSP00000386655.4:n.300+2596C>T
ENST00000409338.5:c.177+6231C>T (RPL36A-HNRNPH2) ENSP00000386974.2:n.177+6231C>T
ENST00000466414.1:n.372G>A (GLA)
ENST00000493905.6:c.*434G>A (GLA) ENSP00000476935.1:n.*434G>A
NM_000169.2:c.1046G>A , LRG_672t1:c.1046G>A (GLA) NP_000160.1:p.Trp349Ter
NM_001199973.1:c.408+2596C>T (RPL36A-HNRNPH2) NP_001186902.1:n.408+2596C>T
NM_001199974.1:c.285+6231C>T (RPL36A-HNRNPH2) NP_001186903.1:n.285+6231C>T
XR_938397.1:n.1131G>A (GLA)
XR_938397.2:n.1152G>A (GLA)
NM_001199973.2:c.300+2596C>T (RPL36A-HNRNPH2) NP_001186902.2:n.300+2596C>T
NM_001199974.2:c.177+6231C>T (RPL36A-HNRNPH2) NP_001186903.2:n.177+6231C>T
NM_000169.3:c.1046G>A (GLA) MANE Select NP_000160.1:p.Trp349Ter
NR_164783.1:n.1125G>A (GLA)