Canonical Allele Identifier: CA2694298375
Gene: GLA HGNC NCBI
RPL36A-HNRNPH2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101398954A>G , CM000685.2:g.101398954A>G GRCh38
NC_000023.10:g.100653942A>G , CM000685.1:g.100653942A>G GRCh37
NC_000023.9:g.100540598A>G NCBI36
NG_007119.1:g.14010T>C , LRG_672:g.14010T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000486121.7:c.*86-8T>C (GLA) ENSP00000501124.2:n.*86-8T>C
ENST00000674127.2:c.*143-8T>C (GLA) ENSP00000501044.2:n.*143-8T>C
ENST00000710365.1:c.715-8T>C (GLA) ENSP00000518234.1:n.715-8T>C
ENST00000218516.4:c.640-8T>C (GLA) MANE Select ENSP00000218516.4:n.640-8T>C
ENST00000466414.2:n.559-8T>C (GLA)
ENST00000468823.2:n.1575-8T>C (GLA)
ENST00000479445.2:n.1037-8T>C (GLA)
ENST00000480513.6:c.548-8T>C (GLA) ENSP00000497055.1:n.548-8T>C
ENST00000486121.6:c.685-8T>C (GLA)
ENST00000649178.1:c.763-8T>C (GLA) ENSP00000498186.1:n.763-8T>C
ENST00000674127.1:c.740-8T>C (GLA) ENSP00000501044.1:n.740-8T>C
ENST00000674142.1:n.727-8T>C (GLA)
ENST00000674634.2:c.640-8T>C (GLA) ENSP00000502629.2:n.640-8T>C
ENST00000675592.1:c.640-8T>C (GLA) ENSP00000502239.1:n.640-8T>C
ENST00000675799.1:c.548-8T>C (GLA) ENSP00000502661.1:n.548-8T>C
ENST00000675968.1:n.3286T>C (GLA)
ENST00000676156.1:c.604-8T>C (GLA) ENSP00000501730.1:n.604-8T>C
ENST00000676372.1:c.640-8T>C (GLA) ENSP00000502805.1:n.640-8T>C
ENST00000218516.3:c.640-8T>C (GLA) ENSP00000218516.3:n.640-8T>C
ENST00000409170.3:c.300+3497A>G (RPL36A-HNRNPH2) ENSP00000386655.4:n.300+3497A>G
ENST00000409338.5:c.177+7132A>G (RPL36A-HNRNPH2) ENSP00000386974.2:n.177+7132A>G
ENST00000468823.1:n.189-8T>C (GLA)
ENST00000480513.5:n.478-8T>C (GLA)
ENST00000486121.5:n.685-8T>C (GLA)
ENST00000493905.6:c.*28-8T>C (GLA) ENSP00000476935.1:n.*28-8T>C
NM_000169.2:c.640-8T>C , LRG_672t1:c.640-8T>C (GLA) NP_000160.1:n.640-8T>C
NM_001199973.1:c.408+3497A>G (RPL36A-HNRNPH2) NP_001186902.1:n.408+3497A>G
NM_001199974.1:c.285+7132A>G (RPL36A-HNRNPH2) NP_001186903.1:n.285+7132A>G
XR_938397.1:n.725-8T>C (GLA)
XR_938397.2:n.746-8T>C (GLA)
NM_001199973.2:c.300+3497A>G (RPL36A-HNRNPH2) NP_001186902.2:n.300+3497A>G
NM_001199974.2:c.177+7132A>G (RPL36A-HNRNPH2) NP_001186903.2:n.177+7132A>G
NM_000169.3:c.640-8T>C (GLA) MANE Select NP_000160.1:n.640-8T>C
NR_164783.1:n.719-8T>C (GLA)