Canonical Allele Identifier: CA658799814
Gene: GLA HGNC NCBI
RPL36A-HNRNPH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 524214
ClinVar RCV Id: RCV000627819
dbSNP Id: rs1555985200

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101398947del , CM000685.2:g.101398947del GRCh38
NC_000023.10:g.100653935del , CM000685.1:g.100653935del GRCh37
NC_000023.9:g.100540591del NCBI36
NG_007119.1:g.14017del , LRG_672:g.14017del

Transcript Alleles

HGVS Amino-acid change
ENST00000486121.7:c.*86-1del (GLA) ENSP00000501124.2:n.*86-1del
ENST00000674127.2:c.*143-1del (GLA) ENSP00000501044.2:n.*143-1del
ENST00000710365.1:c.715-1del (GLA) ENSP00000518234.1:n.715-1del
ENST00000218516.4:c.640-1del (GLA) MANE Select ENSP00000218516.4:n.640-1del
ENST00000466414.2:n.559-1del (GLA)
ENST00000468823.2:n.1575-1del (GLA)
ENST00000479445.2:n.1037-1del (GLA)
ENST00000480513.6:c.548-1del (GLA) ENSP00000497055.1:n.548-1del
ENST00000486121.6:c.685-1del (GLA)
ENST00000649178.1:c.763-1del (GLA) ENSP00000498186.1:n.763-1del
ENST00000674127.1:c.740-1del (GLA) ENSP00000501044.1:n.740-1del
ENST00000674142.1:n.727-1del (GLA)
ENST00000674634.2:c.640-1del (GLA) ENSP00000502629.2:n.640-1del
ENST00000675592.1:c.640-1del (GLA) ENSP00000502239.1:n.640-1del
ENST00000675799.1:c.548-1del (GLA) ENSP00000502661.1:n.548-1del
ENST00000675968.1:n.3293del (GLA)
ENST00000676156.1:c.604-1del (GLA) ENSP00000501730.1:n.604-1del
ENST00000676372.1:c.640-1del (GLA) ENSP00000502805.1:n.640-1del
ENST00000218516.3:c.640-1del (GLA) ENSP00000218516.3:n.640-1del
ENST00000409170.3:c.300+3490del (RPL36A-HNRNPH2) ENSP00000386655.4:n.300+3490del
ENST00000409338.5:c.177+7125del (RPL36A-HNRNPH2) ENSP00000386974.2:n.177+7125del
ENST00000468823.1:n.189-1del (GLA)
ENST00000480513.5:n.478-1del (GLA)
ENST00000486121.5:n.685-1del (GLA)
ENST00000493905.6:c.*28-1del (GLA) ENSP00000476935.1:n.*28-1del
NM_000169.2:c.640-1del , LRG_672t1:c.640-1del (GLA) NP_000160.1:n.640-1del
NM_001199973.1:c.408+3490del (RPL36A-HNRNPH2) NP_001186902.1:n.408+3490del
NM_001199974.1:c.285+7125del (RPL36A-HNRNPH2) NP_001186903.1:n.285+7125del
XR_938397.1:n.725-1del (GLA)
XR_938397.2:n.746-1del (GLA)
NM_001199973.2:c.300+3490del (RPL36A-HNRNPH2) NP_001186902.2:n.300+3490del
NM_001199974.2:c.177+7125del (RPL36A-HNRNPH2) NP_001186903.2:n.177+7125del
NM_000169.3:c.640-1del (GLA) MANE Select NP_000160.1:n.640-1del
NR_164783.1:n.719-1del (GLA)