Canonical Allele Identifier: CA413927311
Gene: GLA HGNC NCBI
RPL36A-HNRNPH2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101400697T>A , CM000685.2:g.101400697T>A GRCh38
NC_000023.10:g.100655685T>A , CM000685.1:g.100655685T>A GRCh37
NC_000023.9:g.100542341T>A NCBI36
NG_007119.1:g.12267A>T , LRG_672:g.12267A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000486121.7:c.*54A>T (GLA) ENSP00000501124.2:n.*54A>T
ENST00000674127.2:c.*54A>T (GLA) ENSP00000501044.2:n.*54A>T
ENST00000710365.1:c.683A>T (GLA) ENSP00000518234.1:p.Glu228Val
ENST00000218516.4:c.608A>T (GLA) MANE Select ENSP00000218516.4:p.Glu203Val
ENST00000466414.2:n.527A>T (GLA)
ENST00000468823.2:n.1543A>T (GLA)
ENST00000479445.2:n.1005A>T (GLA)
ENST00000480513.6:c.547+935A>T (GLA) ENSP00000497055.1:n.547+935A>T
ENST00000486121.6:c.653A>T (GLA)
ENST00000649178.1:c.731A>T (GLA) ENSP00000498186.1:p.Glu244Val
ENST00000674127.1:c.651A>T (GLA) ENSP00000501044.1:n.651A>T
ENST00000674142.1:n.695A>T (GLA)
ENST00000674634.2:c.608A>T (GLA) ENSP00000502629.2:p.Glu203Val
ENST00000675592.1:c.608A>T (GLA) ENSP00000502239.1:p.Glu203Val
ENST00000675799.1:c.547+935A>T (GLA) ENSP00000502661.1:n.547+935A>T
ENST00000675968.1:n.1543A>T (GLA)
ENST00000676156.1:c.572A>T (GLA) ENSP00000501730.1:p.Glu191Val
ENST00000676372.1:c.608A>T (GLA) ENSP00000502805.1:p.Glu203Val
ENST00000218516.3:c.608A>T (GLA) ENSP00000218516.3:p.Glu203Val
ENST00000409170.3:c.300+5240T>A (RPL36A-HNRNPH2) ENSP00000386655.4:n.300+5240T>A
ENST00000409338.5:c.177+8875T>A (RPL36A-HNRNPH2) ENSP00000386974.2:n.177+8875T>A
ENST00000468823.1:n.157A>T (GLA)
ENST00000480513.5:n.477+935A>T (GLA)
ENST00000486121.5:n.653A>T (GLA)
ENST00000493905.6:c.608A>T (GLA) ENSP00000476935.1:p.Glu203Val
NM_000169.2:c.608A>T , LRG_672t1:c.608A>T (GLA) NP_000160.1:p.Glu203Val
NM_001199973.1:c.408+5240T>A (RPL36A-HNRNPH2) NP_001186902.1:n.408+5240T>A
NM_001199974.1:c.285+8875T>A (RPL36A-HNRNPH2) NP_001186903.1:n.285+8875T>A
XR_938397.1:n.636A>T (GLA)
XR_938397.2:n.657A>T (GLA)
NM_001199973.2:c.300+5240T>A (RPL36A-HNRNPH2) NP_001186902.2:n.300+5240T>A
NM_001199974.2:c.177+8875T>A (RPL36A-HNRNPH2) NP_001186903.2:n.177+8875T>A
NM_000169.3:c.608A>T (GLA) MANE Select NP_000160.1:p.Glu203Val
NR_164783.1:n.630A>T (GLA)