Canonical Allele Identifier: CA353055
Gene: GLA HGNC NCBI
RPL36A-HNRNPH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 217404
dbSNP Id: rs869312157

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101398422A>G , CM000685.2:g.101398422A>G GRCh38
NC_000023.10:g.100653410A>G , CM000685.1:g.100653410A>G GRCh37
NC_000023.9:g.100540066A>G NCBI36
NG_007119.1:g.14542T>C , LRG_672:g.14542T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000486121.7:c.*393T>C (GLA) ENSP00000501124.2:n.*393T>C
ENST00000674127.2:c.*450T>C (GLA) ENSP00000501044.2:n.*450T>C
ENST00000710365.1:c.1022T>C (GLA) ENSP00000518234.1:p.Val341Ala
ENST00000218516.4:c.947T>C (GLA) MANE Select ENSP00000218516.4:p.Val316Ala
ENST00000466414.2:n.1083T>C (GLA)
ENST00000468823.2:n.2099T>C (GLA)
ENST00000479445.2:n.1561T>C (GLA)
ENST00000480513.6:c.*255T>C (GLA) ENSP00000497055.1:n.*255T>C
ENST00000486121.6:c.992T>C (GLA)
ENST00000649178.1:c.1070T>C (GLA) ENSP00000498186.1:p.Val357Ala
ENST00000674127.1:c.1047T>C (GLA) ENSP00000501044.1:n.1047T>C
ENST00000674142.1:n.1251T>C (GLA)
ENST00000674634.2:c.947T>C (GLA) ENSP00000502629.2:p.Val316Ala
ENST00000675592.1:c.802-323T>C (GLA) ENSP00000502239.1:n.802-323T>C
ENST00000675799.1:c.*472T>C (GLA) ENSP00000502661.1:n.*472T>C
ENST00000675968.1:n.3818T>C (GLA)
ENST00000676156.1:c.911T>C (GLA) ENSP00000501730.1:p.Val304Ala
ENST00000676372.1:c.1013T>C (GLA) ENSP00000502805.1:n.1013T>C
ENST00000218516.3:c.947T>C (GLA) ENSP00000218516.3:p.Val316Ala
ENST00000409170.3:c.300+2965A>G (RPL36A-HNRNPH2) ENSP00000386655.4:n.300+2965A>G
ENST00000409338.5:c.177+6600A>G (RPL36A-HNRNPH2) ENSP00000386974.2:n.177+6600A>G
ENST00000466414.1:n.273T>C (GLA)
ENST00000493905.6:c.*335T>C (GLA) ENSP00000476935.1:n.*335T>C
NM_000169.2:c.947T>C , LRG_672t1:c.947T>C (GLA) NP_000160.1:p.Val316Ala
NM_001199973.1:c.408+2965A>G (RPL36A-HNRNPH2) NP_001186902.1:n.408+2965A>G
NM_001199974.1:c.285+6600A>G (RPL36A-HNRNPH2) NP_001186903.1:n.285+6600A>G
XR_938397.1:n.1032T>C (GLA)
XR_938397.2:n.1053T>C (GLA)
NM_001199973.2:c.300+2965A>G (RPL36A-HNRNPH2) NP_001186902.2:n.300+2965A>G
NM_001199974.2:c.177+6600A>G (RPL36A-HNRNPH2) NP_001186903.2:n.177+6600A>G
NM_000169.3:c.947T>C (GLA) MANE Select NP_000160.1:p.Val316Ala
NR_164783.1:n.1026T>C (GLA)