Canonical Allele Identifier: CA021455

Gene: GLA RPL36A-HNRNPH2

Linked Data

• ClinVar Variation Id: 92539
• ClinVar RCV Id: RCV000078264 ; RCV003997194
• dbSNP Id: rs398123199
• MyVariant Identifiers: chrX:g.100662773G>C (hg19) ; chrX:g.101407785G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.101407785G>C , CM000685.2:g.101407785G>C	GRCh38
NC_000023.10:g.100662773G>C , CM000685.1:g.100662773G>C	GRCh37
NC_000023.9:g.100549429G>C	NCBI36
NG_007119.1:g.5179C>G , LRG_672:g.5179C>G
NG_016327.1:g.4583G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000486121.7:c.119C>G (GLA)	ENSP00000501124.2:p.Pro40Arg
ENST00000674127.2:c.119C>G (GLA)	ENSP00000501044.2:p.Pro40Arg
ENST00000710365.1:c.119C>G (GLA)	ENSP00000518234.1:p.Pro40Arg
ENST00000218516.4:c.119C>G (GLA) MANE Select	ENSP00000218516.4:p.Pro40Arg
ENST00000466414.2:n.38C>G (GLA)
ENST00000468823.2:n.180C>G (GLA)
ENST00000479445.2:n.117C>G (GLA)
ENST00000480513.6:c.119C>G (GLA)	ENSP00000497055.1:p.Pro40Arg
ENST00000486121.6:c.49C>G (GLA)
ENST00000649178.1:c.119C>G (GLA)	ENSP00000498186.1:p.Pro40Arg
ENST00000674127.1:c.47C>G (GLA)	ENSP00000501044.1:p.Pro16Arg
ENST00000674142.1:n.206C>G (GLA)
ENST00000674634.2:c.119C>G (GLA)	ENSP00000502629.2:p.Pro40Arg
ENST00000675592.1:c.119C>G (GLA)	ENSP00000502239.1:p.Pro40Arg
ENST00000675799.1:c.119C>G (GLA)	ENSP00000502661.1:p.Pro40Arg
ENST00000675968.1:n.180C>G (GLA)
ENST00000676156.1:c.119C>G (GLA)	ENSP00000501730.1:p.Pro40Arg
ENST00000676372.1:c.119C>G (GLA)	ENSP00000502805.1:p.Pro40Arg
ENST00000218516.3:c.119C>G (GLA)	ENSP00000218516.3:p.Pro40Arg
ENST00000409170.3:c.301-4151G>C (RPL36A-HNRNPH2)	ENSP00000386655.4:n.301-4151G>C
ENST00000409338.5:c.178-4151G>C (RPL36A-HNRNPH2)	ENSP00000386974.2:n.178-4151G>C
ENST00000479445.1:n.103C>G (GLA)
ENST00000480513.5:n.49C>G (GLA)
ENST00000486121.5:n.49C>G (GLA)
ENST00000493905.6:c.119C>G (GLA)	ENSP00000476935.1:p.Pro40Arg
NM_000169.2:c.119C>G , LRG_672t1:c.119C>G (GLA)	NP_000160.1:p.Pro40Arg
NM_001199973.1:c.409-4151G>C (RPL36A-HNRNPH2)	NP_001186902.1:n.409-4151G>C
NM_001199974.1:c.286-4151G>C (RPL36A-HNRNPH2)	NP_001186903.1:n.286-4151G>C
XR_938397.1:n.147C>G (GLA)
XR_938397.2:n.168C>G (GLA)
NM_001199973.2:c.301-4151G>C (RPL36A-HNRNPH2)	NP_001186902.2:n.301-4151G>C
NM_001199974.2:c.178-4151G>C (RPL36A-HNRNPH2)	NP_001186903.2:n.178-4151G>C
NM_000169.3:c.119C>G (GLA) MANE Select	NP_000160.1:p.Pro40Arg
NR_164783.1:n.141C>G (GLA)