Canonical Allele Identifier: CA413937907
Gene: GLA HGNC NCBI
RPL36A-HNRNPH2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101407893C>G , CM000685.2:g.101407893C>G GRCh38
NC_000023.10:g.100662881C>G , CM000685.1:g.100662881C>G GRCh37
NC_000023.9:g.100549537C>G NCBI36
NG_007119.1:g.5071G>C , LRG_672:g.5071G>C
NG_016327.1:g.4691C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000486121.7:c.11G>C (GLA) ENSP00000501124.2:p.Arg4Thr
ENST00000674127.2:c.11G>C (GLA) ENSP00000501044.2:p.Arg4Thr
ENST00000710365.1:c.11G>C (GLA) ENSP00000518234.1:p.Arg4Thr
ENST00000218516.4:c.11G>C (GLA) MANE Select ENSP00000218516.4:p.Arg4Thr
ENST00000468823.2:n.72G>C (GLA)
ENST00000479445.2:n.9G>C (GLA)
ENST00000480513.6:c.11G>C (GLA) ENSP00000497055.1:p.Arg4Thr
ENST00000649178.1:c.11G>C (GLA) ENSP00000498186.1:p.Arg4Thr
ENST00000674142.1:n.98G>C (GLA)
ENST00000674634.2:c.11G>C (GLA) ENSP00000502629.2:p.Arg4Thr
ENST00000675592.1:c.11G>C (GLA) ENSP00000502239.1:p.Arg4Thr
ENST00000675799.1:c.11G>C (GLA) ENSP00000502661.1:p.Arg4Thr
ENST00000675968.1:n.72G>C (GLA)
ENST00000676156.1:c.11G>C (GLA) ENSP00000501730.1:p.Arg4Thr
ENST00000676372.1:c.11G>C (GLA) ENSP00000502805.1:p.Arg4Thr
ENST00000218516.3:c.11G>C (GLA) ENSP00000218516.3:p.Arg4Thr
ENST00000409170.3:c.301-4043C>G (RPL36A-HNRNPH2) ENSP00000386655.4:n.301-4043C>G
ENST00000409338.5:c.178-4043C>G (RPL36A-HNRNPH2) ENSP00000386974.2:n.178-4043C>G
ENST00000493905.6:c.11G>C (GLA) ENSP00000476935.1:p.Arg4Thr
NM_000169.2:c.11G>C , LRG_672t1:c.11G>C (GLA) NP_000160.1:p.Arg4Thr
NM_001199973.1:c.409-4043C>G (RPL36A-HNRNPH2) NP_001186902.1:n.409-4043C>G
NM_001199974.1:c.286-4043C>G (RPL36A-HNRNPH2) NP_001186903.1:n.286-4043C>G
XR_938397.1:n.39G>C (GLA)
XR_938397.2:n.60G>C (GLA)
NM_001199973.2:c.301-4043C>G (RPL36A-HNRNPH2) NP_001186902.2:n.301-4043C>G
NM_001199974.2:c.178-4043C>G (RPL36A-HNRNPH2) NP_001186903.2:n.178-4043C>G
NM_000169.3:c.11G>C (GLA) MANE Select NP_000160.1:p.Arg4Thr
NR_164783.1:n.33G>C (GLA)