Canonical Allele Identifier: CA2448298177
Gene: GLA HGNC NCBI
RPL36A-HNRNPH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101398841T= , CM000685.2:g.101398841T= GRCh38
NC_000023.10:g.100653829T= , CM000685.1:g.100653829T= GRCh37
NC_000023.9:g.100540485T= NCBI36
NG_007119.1:g.14123A= , LRG_672:g.14123A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000486121.7:c.*191A= (GLA) ENSP00000501124.2:n.*191A=
ENST00000674127.2:c.*248A= (GLA) ENSP00000501044.2:n.*248A=
ENST00000710365.1:c.820A= (GLA) ENSP00000518234.1:p.Asn274=
ENST00000218516.4:c.745A= (GLA) MANE Select ENSP00000218516.4:p.Asn249=
ENST00000466414.2:n.664A= (GLA)
ENST00000468823.2:n.1680A= (GLA)
ENST00000479445.2:n.1142A= (GLA)
ENST00000480513.6:c.*53A= (GLA) ENSP00000497055.1:n.*53A=
ENST00000486121.6:c.790A= (GLA)
ENST00000649178.1:c.868A= (GLA) ENSP00000498186.1:p.Asn290=
ENST00000674127.1:c.845A= (GLA) ENSP00000501044.1:n.845A=
ENST00000674142.1:n.832A= (GLA)
ENST00000674634.2:c.745A= (GLA) ENSP00000502629.2:p.Asn249=
ENST00000675592.1:c.745A= (GLA) ENSP00000502239.1:p.Asn249=
ENST00000675799.1:c.*53A= (GLA) ENSP00000502661.1:n.*53A=
ENST00000675968.1:n.3399A= (GLA)
ENST00000676156.1:c.709A= (GLA) ENSP00000501730.1:p.Asn237=
ENST00000676372.1:c.745A= (GLA) ENSP00000502805.1:p.Asn249=
ENST00000218516.3:c.745A= (GLA) ENSP00000218516.3:p.Asn249=
ENST00000409170.3:c.300+3384T= (RPL36A-HNRNPH2) ENSP00000386655.4:n.300+3384T=
ENST00000409338.5:c.177+7019T= (RPL36A-HNRNPH2) ENSP00000386974.2:n.177+7019T=
ENST00000468823.1:n.294A= (GLA)
ENST00000480513.5:n.583A= (GLA)
ENST00000493905.6:c.*133A= (GLA) ENSP00000476935.1:n.*133A=
NM_000169.2:c.745A= , LRG_672t1:c.745A= (GLA) NP_000160.1:p.Asn249=
NM_001199973.1:c.408+3384T= (RPL36A-HNRNPH2) NP_001186902.1:n.408+3384T=
NM_001199974.1:c.285+7019T= (RPL36A-HNRNPH2) NP_001186903.1:n.285+7019T=
XR_938397.1:n.830A= (GLA)
XR_938397.2:n.851A= (GLA)
NM_001199973.2:c.300+3384T= (RPL36A-HNRNPH2) NP_001186902.2:n.300+3384T=
NM_001199974.2:c.177+7019T= (RPL36A-HNRNPH2) NP_001186903.2:n.177+7019T=
NM_000169.3:c.745A= (GLA) MANE Select NP_000160.1:p.Asn249=
NR_164783.1:n.824A= (GLA)