Canonical Allele Identifier: CA2448298175
Gene: GLA HGNC NCBI
RPL36A-HNRNPH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101398839G= , CM000685.2:g.101398839G= GRCh38
NC_000023.10:g.100653827G= , CM000685.1:g.100653827G= GRCh37
NC_000023.9:g.100540483G= NCBI36
NG_007119.1:g.14125C= , LRG_672:g.14125C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000486121.7:c.*193C= (GLA) ENSP00000501124.2:n.*193C=
ENST00000674127.2:c.*250C= (GLA) ENSP00000501044.2:n.*250C=
ENST00000710365.1:c.822C= (GLA) ENSP00000518234.1:p.Asn274=
ENST00000218516.4:c.747C= (GLA) MANE Select ENSP00000218516.4:p.Asn249=
ENST00000466414.2:n.666C= (GLA)
ENST00000468823.2:n.1682C= (GLA)
ENST00000479445.2:n.1144C= (GLA)
ENST00000480513.6:c.*55C= (GLA) ENSP00000497055.1:n.*55C=
ENST00000486121.6:c.792C= (GLA)
ENST00000649178.1:c.870C= (GLA) ENSP00000498186.1:p.Asn290=
ENST00000674127.1:c.847C= (GLA) ENSP00000501044.1:n.847C=
ENST00000674142.1:n.834C= (GLA)
ENST00000674634.2:c.747C= (GLA) ENSP00000502629.2:p.Asn249=
ENST00000675592.1:c.747C= (GLA) ENSP00000502239.1:p.Asn249=
ENST00000675799.1:c.*55C= (GLA) ENSP00000502661.1:n.*55C=
ENST00000675968.1:n.3401C= (GLA)
ENST00000676156.1:c.711C= (GLA) ENSP00000501730.1:p.Asn237=
ENST00000676372.1:c.747C= (GLA) ENSP00000502805.1:p.Asn249=
ENST00000218516.3:c.747C= (GLA) ENSP00000218516.3:p.Asn249=
ENST00000409170.3:c.300+3382G= (RPL36A-HNRNPH2) ENSP00000386655.4:n.300+3382G=
ENST00000409338.5:c.177+7017G= (RPL36A-HNRNPH2) ENSP00000386974.2:n.177+7017G=
ENST00000468823.1:n.296C= (GLA)
ENST00000480513.5:n.585C= (GLA)
ENST00000493905.6:c.*135C= (GLA) ENSP00000476935.1:n.*135C=
NM_000169.2:c.747C= , LRG_672t1:c.747C= (GLA) NP_000160.1:p.Asn249=
NM_001199973.1:c.408+3382G= (RPL36A-HNRNPH2) NP_001186902.1:n.408+3382G=
NM_001199974.1:c.285+7017G= (RPL36A-HNRNPH2) NP_001186903.1:n.285+7017G=
XR_938397.1:n.832C= (GLA)
XR_938397.2:n.853C= (GLA)
NM_001199973.2:c.300+3382G= (RPL36A-HNRNPH2) NP_001186902.2:n.300+3382G=
NM_001199974.2:c.177+7017G= (RPL36A-HNRNPH2) NP_001186903.2:n.177+7017G=
NM_000169.3:c.747C= (GLA) MANE Select NP_000160.1:p.Asn249=
NR_164783.1:n.826C= (GLA)