Canonical Allele Identifier: CA2448298830
Gene: GLA HGNC NCBI
RPL36A-HNRNPH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101400705G= , CM000685.2:g.101400705G= GRCh38
NC_000023.10:g.100655693G= , CM000685.1:g.100655693G= GRCh37
NC_000023.9:g.100542349G= NCBI36
NG_007119.1:g.12259C= , LRG_672:g.12259C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000486121.7:c.*46C= (GLA) ENSP00000501124.2:n.*46C=
ENST00000674127.2:c.*46C= (GLA) ENSP00000501044.2:n.*46C=
ENST00000710365.1:c.675C= (GLA) ENSP00000518234.1:p.Tyr225=
ENST00000218516.4:c.600C= (GLA) MANE Select ENSP00000218516.4:p.Tyr200=
ENST00000466414.2:n.519C= (GLA)
ENST00000468823.2:n.1535C= (GLA)
ENST00000479445.2:n.997C= (GLA)
ENST00000480513.6:c.547+927C= (GLA) ENSP00000497055.1:n.547+927C=
ENST00000486121.6:c.645C= (GLA)
ENST00000649178.1:c.723C= (GLA) ENSP00000498186.1:p.Tyr241=
ENST00000674127.1:c.643C= (GLA) ENSP00000501044.1:n.643C=
ENST00000674142.1:n.687C= (GLA)
ENST00000674634.2:c.600C= (GLA) ENSP00000502629.2:p.Tyr200=
ENST00000675592.1:c.600C= (GLA) ENSP00000502239.1:p.Tyr200=
ENST00000675799.1:c.547+927C= (GLA) ENSP00000502661.1:n.547+927C=
ENST00000675968.1:n.1535C= (GLA)
ENST00000676156.1:c.564C= (GLA) ENSP00000501730.1:p.Tyr188=
ENST00000676372.1:c.600C= (GLA) ENSP00000502805.1:p.Tyr200=
ENST00000218516.3:c.600C= (GLA) ENSP00000218516.3:p.Tyr200=
ENST00000409170.3:c.300+5248G= (RPL36A-HNRNPH2) ENSP00000386655.4:n.300+5248G=
ENST00000409338.5:c.177+8883G= (RPL36A-HNRNPH2) ENSP00000386974.2:n.177+8883G=
ENST00000468823.1:n.149C= (GLA)
ENST00000480513.5:n.477+927C= (GLA)
ENST00000486121.5:n.645C= (GLA)
ENST00000493905.6:c.600C= (GLA) ENSP00000476935.1:p.Tyr200=
NM_000169.2:c.600C= , LRG_672t1:c.600C= (GLA) NP_000160.1:p.Tyr200=
NM_001199973.1:c.408+5248G= (RPL36A-HNRNPH2) NP_001186902.1:n.408+5248G=
NM_001199974.1:c.285+8883G= (RPL36A-HNRNPH2) NP_001186903.1:n.285+8883G=
XR_938397.1:n.628C= (GLA)
XR_938397.2:n.649C= (GLA)
NM_001199973.2:c.300+5248G= (RPL36A-HNRNPH2) NP_001186902.2:n.300+5248G=
NM_001199974.2:c.177+8883G= (RPL36A-HNRNPH2) NP_001186903.2:n.177+8883G=
NM_000169.3:c.600C= (GLA) MANE Select NP_000160.1:p.Tyr200=
NR_164783.1:n.622C= (GLA)