Canonical Allele Identifier: CA2695234874
Gene: GLA HGNC NCBI
RPL36A-HNRNPH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101397999dup , CM000685.2:g.101397999dup GRCh38
NC_000023.10:g.100652987dup , CM000685.1:g.100652987dup GRCh37
NC_000023.9:g.100539643dup NCBI36
NG_007119.1:g.14965dup , LRG_672:g.14965dup

Transcript Alleles

HGVS Amino-acid change
ENST00000486121.7:c.*546dup (GLA) ENSP00000501124.2:n.*546dup
ENST00000674127.2:c.*603dup (GLA) ENSP00000501044.2:n.*603dup
ENST00000710365.1:c.1175dup (GLA) ENSP00000518234.1:p.Ala393ArgfsTer7
ENST00000218516.4:c.1100dup (GLA) MANE Select ENSP00000218516.4:p.Ala368ArgfsTer7
ENST00000466414.2:n.1236dup (GLA)
ENST00000468823.2:n.2522dup (GLA)
ENST00000479445.2:n.1714dup (GLA)
ENST00000480513.6:c.*408dup (GLA) ENSP00000497055.1:n.*408dup
ENST00000486121.6:c.1145dup (GLA)
ENST00000649178.1:c.1223dup (GLA) ENSP00000498186.1:p.Ala409ArgfsTer7
ENST00000674127.1:c.1200dup (GLA) ENSP00000501044.1:n.1200dup
ENST00000674142.1:n.1404dup (GLA)
ENST00000675592.1:c.902dup (GLA) ENSP00000502239.1:p.Ala302ArgfsTer7
ENST00000675799.1:c.*625dup (GLA) ENSP00000502661.1:n.*625dup
ENST00000675968.1:n.3971dup (GLA)
ENST00000676156.1:c.1064dup (GLA) ENSP00000501730.1:p.Ala356ArgfsTer7
ENST00000676372.1:c.1166dup (GLA) ENSP00000502805.1:n.1166dup
ENST00000218516.3:c.1100dup (GLA) ENSP00000218516.3:p.Ala368ArgfsTer7
ENST00000409170.3:c.300+2542dup (RPL36A-HNRNPH2) ENSP00000386655.4:n.300+2542dup
ENST00000409338.5:c.177+6177dup (RPL36A-HNRNPH2) ENSP00000386974.2:n.177+6177dup
ENST00000466414.1:n.426dup (GLA)
ENST00000493905.6:c.*488dup (GLA) ENSP00000476935.1:n.*488dup
NM_000169.2:c.1100dup , LRG_672t1:c.1100dup (GLA) NP_000160.1:p.Ala368ArgfsTer7
NM_001199973.1:c.408+2542dup (RPL36A-HNRNPH2) NP_001186902.1:n.408+2542dup
NM_001199974.1:c.285+6177dup (RPL36A-HNRNPH2) NP_001186903.1:n.285+6177dup
XR_938397.1:n.1185dup (GLA)
XR_938397.2:n.1206dup (GLA)
NM_001199973.2:c.300+2542dup (RPL36A-HNRNPH2) NP_001186902.2:n.300+2542dup
NM_001199974.2:c.177+6177dup (RPL36A-HNRNPH2) NP_001186903.2:n.177+6177dup
NM_000169.3:c.1100dup (GLA) MANE Select NP_000160.1:p.Ala368ArgfsTer7
NR_164783.1:n.1179dup (GLA)