Canonical Allele Identifier: CA413923237

Gene: GLA RPL36A-HNRNPH2

Linked Data

• MyVariant Identifiers: chrX:g.100653531T>G (hg19) ; chrX:g.101398543T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.101398543T>G , CM000685.2:g.101398543T>G	GRCh38
NC_000023.10:g.100653531T>G , CM000685.1:g.100653531T>G	GRCh37
NC_000023.9:g.100540187T>G	NCBI36
NG_007119.1:g.14421A>C , LRG_672:g.14421A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000486121.7:c.*272A>C (GLA)	ENSP00000501124.2:n.*272A>C
ENST00000674127.2:c.*329A>C (GLA)	ENSP00000501044.2:n.*329A>C
ENST00000710365.1:c.901A>C (GLA)	ENSP00000518234.1:p.Ser301Arg
ENST00000218516.4:c.826A>C (GLA) MANE Select	ENSP00000218516.4:p.Ser276Arg
ENST00000466414.2:n.962A>C (GLA)
ENST00000468823.2:n.1978A>C (GLA)
ENST00000479445.2:n.1440A>C (GLA)
ENST00000480513.6:c.*134A>C (GLA)	ENSP00000497055.1:n.*134A>C
ENST00000486121.6:c.871A>C (GLA)
ENST00000649178.1:c.949A>C (GLA)	ENSP00000498186.1:p.Ser317Arg
ENST00000674127.1:c.926A>C (GLA)	ENSP00000501044.1:n.926A>C
ENST00000674142.1:n.1130A>C (GLA)
ENST00000674634.2:c.826A>C (GLA)	ENSP00000502629.2:p.Ser276Arg
ENST00000675592.1:c.801+242A>C (GLA)	ENSP00000502239.1:n.801+242A>C
ENST00000675799.1:c.*351A>C (GLA)	ENSP00000502661.1:n.*351A>C
ENST00000675968.1:n.3697A>C (GLA)
ENST00000676156.1:c.790A>C (GLA)	ENSP00000501730.1:p.Ser264Arg
ENST00000676372.1:c.892A>C (GLA)	ENSP00000502805.1:n.892A>C
ENST00000218516.3:c.826A>C (GLA)	ENSP00000218516.3:p.Ser276Arg
ENST00000409170.3:c.300+3086T>G (RPL36A-HNRNPH2)	ENSP00000386655.4:n.300+3086T>G
ENST00000409338.5:c.177+6721T>G (RPL36A-HNRNPH2)	ENSP00000386974.2:n.177+6721T>G
ENST00000466414.1:n.152A>C (GLA)
ENST00000468823.1:n.592A>C (GLA)
ENST00000493905.6:c.*214A>C (GLA)	ENSP00000476935.1:n.*214A>C
NM_000169.2:c.826A>C , LRG_672t1:c.826A>C (GLA)	NP_000160.1:p.Ser276Arg
NM_001199973.1:c.408+3086T>G (RPL36A-HNRNPH2)	NP_001186902.1:n.408+3086T>G
NM_001199974.1:c.285+6721T>G (RPL36A-HNRNPH2)	NP_001186903.1:n.285+6721T>G
XR_938397.1:n.911A>C (GLA)
XR_938397.2:n.932A>C (GLA)
NM_001199973.2:c.300+3086T>G (RPL36A-HNRNPH2)	NP_001186902.2:n.300+3086T>G
NM_001199974.2:c.177+6721T>G (RPL36A-HNRNPH2)	NP_001186903.2:n.177+6721T>G
NM_000169.3:c.826A>C (GLA) MANE Select	NP_000160.1:p.Ser276Arg
NR_164783.1:n.905A>C (GLA)