Canonical Allele Identifier: CA2448298238
Gene: GLA HGNC NCBI
RPL36A-HNRNPH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101398945G= , CM000685.2:g.101398945G= GRCh38
NC_000023.10:g.100653933G= , CM000685.1:g.100653933G= GRCh37
NC_000023.9:g.100540589G= NCBI36
NG_007119.1:g.14019C= , LRG_672:g.14019C=

Transcript Alleles

HGVS Amino-acid change
ENST00000486121.7:c.*87C= (GLA) ENSP00000501124.2:n.*87C=
ENST00000674127.2:c.*144C= (GLA) ENSP00000501044.2:n.*144C=
ENST00000710365.1:c.716C= (GLA) ENSP00000518234.1:p.Pro239=
ENST00000218516.4:c.641C= (GLA) MANE Select ENSP00000218516.4:p.Pro214=
ENST00000466414.2:n.560C= (GLA)
ENST00000468823.2:n.1576C= (GLA)
ENST00000479445.2:n.1038C= (GLA)
ENST00000480513.6:c.549C= (GLA) ENSP00000497055.1:p.Ala183=
ENST00000486121.6:c.686C= (GLA)
ENST00000649178.1:c.764C= (GLA) ENSP00000498186.1:p.Pro255=
ENST00000674127.1:c.741C= (GLA) ENSP00000501044.1:n.741C=
ENST00000674142.1:n.728C= (GLA)
ENST00000674634.2:c.641C= (GLA) ENSP00000502629.2:p.Pro214=
ENST00000675592.1:c.641C= (GLA) ENSP00000502239.1:p.Pro214=
ENST00000675799.1:c.549C= (GLA) ENSP00000502661.1:p.Ala183=
ENST00000675968.1:n.3295C= (GLA)
ENST00000676156.1:c.605C= (GLA) ENSP00000501730.1:p.Pro202=
ENST00000676372.1:c.641C= (GLA) ENSP00000502805.1:p.Pro214=
ENST00000218516.3:c.641C= (GLA) ENSP00000218516.3:p.Pro214=
ENST00000409170.3:c.300+3488G= (RPL36A-HNRNPH2) ENSP00000386655.4:n.300+3488G=
ENST00000409338.5:c.177+7123G= (RPL36A-HNRNPH2) ENSP00000386974.2:n.177+7123G=
ENST00000468823.1:n.190C= (GLA)
ENST00000480513.5:n.479C= (GLA)
ENST00000486121.5:n.686C= (GLA)
ENST00000493905.6:c.*29C= (GLA) ENSP00000476935.1:n.*29C=
NM_000169.2:c.641C= , LRG_672t1:c.641C= (GLA) NP_000160.1:p.Pro214=
NM_001199973.1:c.408+3488G= (RPL36A-HNRNPH2) NP_001186902.1:n.408+3488G=
NM_001199974.1:c.285+7123G= (RPL36A-HNRNPH2) NP_001186903.1:n.285+7123G=
XR_938397.1:n.726C= (GLA)
XR_938397.2:n.747C= (GLA)
NM_001199973.2:c.300+3488G= (RPL36A-HNRNPH2) NP_001186902.2:n.300+3488G=
NM_001199974.2:c.177+7123G= (RPL36A-HNRNPH2) NP_001186903.2:n.177+7123G=
NM_000169.3:c.641C= (GLA) MANE Select NP_000160.1:p.Pro214=
NR_164783.1:n.720C= (GLA)