Canonical Allele Identifier: CA413921055
Gene: GLA HGNC NCBI
RPL36A-HNRNPH2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101398048C>T , CM000685.2:g.101398048C>T GRCh38
NC_000023.10:g.100653036C>T , CM000685.1:g.100653036C>T GRCh37
NC_000023.9:g.100539692C>T NCBI36
NG_007119.1:g.14916G>A , LRG_672:g.14916G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000486121.7:c.*497G>A (GLA) ENSP00000501124.2:n.*497G>A
ENST00000674127.2:c.*554G>A (GLA) ENSP00000501044.2:n.*554G>A
ENST00000710365.1:c.1126G>A (GLA) ENSP00000518234.1:p.Val376Ile
ENST00000218516.4:c.1051G>A (GLA) MANE Select ENSP00000218516.4:p.Val351Ile
ENST00000466414.2:n.1187G>A (GLA)
ENST00000468823.2:n.2473G>A (GLA)
ENST00000479445.2:n.1665G>A (GLA)
ENST00000480513.6:c.*359G>A (GLA) ENSP00000497055.1:n.*359G>A
ENST00000486121.6:c.1096G>A (GLA)
ENST00000649178.1:c.1174G>A (GLA) ENSP00000498186.1:p.Val392Ile
ENST00000674127.1:c.1151G>A (GLA) ENSP00000501044.1:n.1151G>A
ENST00000674142.1:n.1355G>A (GLA)
ENST00000675592.1:c.853G>A (GLA) ENSP00000502239.1:p.Val285Ile
ENST00000675799.1:c.*576G>A (GLA) ENSP00000502661.1:n.*576G>A
ENST00000675968.1:n.3922G>A (GLA)
ENST00000676156.1:c.1015G>A (GLA) ENSP00000501730.1:p.Val339Ile
ENST00000676372.1:c.1117G>A (GLA) ENSP00000502805.1:n.1117G>A
ENST00000218516.3:c.1051G>A (GLA) ENSP00000218516.3:p.Val351Ile
ENST00000409170.3:c.300+2591C>T (RPL36A-HNRNPH2) ENSP00000386655.4:n.300+2591C>T
ENST00000409338.5:c.177+6226C>T (RPL36A-HNRNPH2) ENSP00000386974.2:n.177+6226C>T
ENST00000466414.1:n.377G>A (GLA)
ENST00000493905.6:c.*439G>A (GLA) ENSP00000476935.1:n.*439G>A
NM_000169.2:c.1051G>A , LRG_672t1:c.1051G>A (GLA) NP_000160.1:p.Val351Ile
NM_001199973.1:c.408+2591C>T (RPL36A-HNRNPH2) NP_001186902.1:n.408+2591C>T
NM_001199974.1:c.285+6226C>T (RPL36A-HNRNPH2) NP_001186903.1:n.285+6226C>T
XR_938397.1:n.1136G>A (GLA)
XR_938397.2:n.1157G>A (GLA)
NM_001199973.2:c.300+2591C>T (RPL36A-HNRNPH2) NP_001186902.2:n.300+2591C>T
NM_001199974.2:c.177+6226C>T (RPL36A-HNRNPH2) NP_001186903.2:n.177+6226C>T
NM_000169.3:c.1051G>A (GLA) MANE Select NP_000160.1:p.Val351Ile
NR_164783.1:n.1130G>A (GLA)