Canonical Allele Identifier: CA2448298182
Gene: GLA HGNC NCBI
RPL36A-HNRNPH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101398852C= , CM000685.2:g.101398852C= GRCh38
NC_000023.10:g.100653840C= , CM000685.1:g.100653840C= GRCh37
NC_000023.9:g.100540496C= NCBI36
NG_007119.1:g.14112G= , LRG_672:g.14112G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000486121.7:c.*180G= (GLA) ENSP00000501124.2:n.*180G=
ENST00000674127.2:c.*237G= (GLA) ENSP00000501044.2:n.*237G=
ENST00000710365.1:c.809G= (GLA) ENSP00000518234.1:p.Trp270=
ENST00000218516.4:c.734G= (GLA) MANE Select ENSP00000218516.4:p.Trp245=
ENST00000466414.2:n.653G= (GLA)
ENST00000468823.2:n.1669G= (GLA)
ENST00000479445.2:n.1131G= (GLA)
ENST00000480513.6:c.*42G= (GLA) ENSP00000497055.1:n.*42G=
ENST00000486121.6:c.779G= (GLA)
ENST00000649178.1:c.857G= (GLA) ENSP00000498186.1:p.Trp286=
ENST00000674127.1:c.834G= (GLA) ENSP00000501044.1:n.834G=
ENST00000674142.1:n.821G= (GLA)
ENST00000674634.2:c.734G= (GLA) ENSP00000502629.2:p.Trp245=
ENST00000675592.1:c.734G= (GLA) ENSP00000502239.1:p.Trp245=
ENST00000675799.1:c.*42G= (GLA) ENSP00000502661.1:n.*42G=
ENST00000675968.1:n.3388G= (GLA)
ENST00000676156.1:c.698G= (GLA) ENSP00000501730.1:p.Trp233=
ENST00000676372.1:c.734G= (GLA) ENSP00000502805.1:p.Trp245=
ENST00000218516.3:c.734G= (GLA) ENSP00000218516.3:p.Trp245=
ENST00000409170.3:c.300+3395C= (RPL36A-HNRNPH2) ENSP00000386655.4:n.300+3395C=
ENST00000409338.5:c.177+7030C= (RPL36A-HNRNPH2) ENSP00000386974.2:n.177+7030C=
ENST00000468823.1:n.283G= (GLA)
ENST00000480513.5:n.572G= (GLA)
ENST00000493905.6:c.*122G= (GLA) ENSP00000476935.1:n.*122G=
NM_000169.2:c.734G= , LRG_672t1:c.734G= (GLA) NP_000160.1:p.Trp245=
NM_001199973.1:c.408+3395C= (RPL36A-HNRNPH2) NP_001186902.1:n.408+3395C=
NM_001199974.1:c.285+7030C= (RPL36A-HNRNPH2) NP_001186903.1:n.285+7030C=
XR_938397.1:n.819G= (GLA)
XR_938397.2:n.840G= (GLA)
NM_001199973.2:c.300+3395C= (RPL36A-HNRNPH2) NP_001186902.2:n.300+3395C=
NM_001199974.2:c.177+7030C= (RPL36A-HNRNPH2) NP_001186903.2:n.177+7030C=
NM_000169.3:c.734G= (GLA) MANE Select NP_000160.1:p.Trp245=
NR_164783.1:n.813G= (GLA)