Canonical Allele Identifier: CA413923427

Gene: GLA RPL36A-HNRNPH2

Linked Data

• gnomAD v4: X-101398558-C-A
• MyVariant Identifiers: chrX:g.100653546C>A (hg19) ; chrX:g.101398558C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.101398558C>A , CM000685.2:g.101398558C>A	GRCh38
NC_000023.10:g.100653546C>A , CM000685.1:g.100653546C>A	GRCh37
NC_000023.9:g.100540202C>A	NCBI36
NG_007119.1:g.14406G>T , LRG_672:g.14406G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000486121.7:c.*257G>T (GLA)	ENSP00000501124.2:n.*257G>T
ENST00000674127.2:c.*314G>T (GLA)	ENSP00000501044.2:n.*314G>T
ENST00000710365.1:c.886G>T (GLA)	ENSP00000518234.1:p.Gly296Cys
ENST00000218516.4:c.811G>T (GLA) MANE Select	ENSP00000218516.4:p.Gly271Cys
ENST00000466414.2:n.947G>T (GLA)
ENST00000468823.2:n.1963G>T (GLA)
ENST00000479445.2:n.1425G>T (GLA)
ENST00000480513.6:c.*119G>T (GLA)	ENSP00000497055.1:n.*119G>T
ENST00000486121.6:c.856G>T (GLA)
ENST00000649178.1:c.934G>T (GLA)	ENSP00000498186.1:p.Gly312Cys
ENST00000674127.1:c.911G>T (GLA)	ENSP00000501044.1:n.911G>T
ENST00000674142.1:n.1115G>T (GLA)
ENST00000674634.2:c.811G>T (GLA)	ENSP00000502629.2:p.Gly271Cys
ENST00000675592.1:c.801+227G>T (GLA)	ENSP00000502239.1:n.801+227G>T
ENST00000675799.1:c.*336G>T (GLA)	ENSP00000502661.1:n.*336G>T
ENST00000675968.1:n.3682G>T (GLA)
ENST00000676156.1:c.775G>T (GLA)	ENSP00000501730.1:p.Gly259Cys
ENST00000676372.1:c.877G>T (GLA)	ENSP00000502805.1:n.877G>T
ENST00000218516.3:c.811G>T (GLA)	ENSP00000218516.3:p.Gly271Cys
ENST00000409170.3:c.300+3101C>A (RPL36A-HNRNPH2)	ENSP00000386655.4:n.300+3101C>A
ENST00000409338.5:c.177+6736C>A (RPL36A-HNRNPH2)	ENSP00000386974.2:n.177+6736C>A
ENST00000466414.1:n.137G>T (GLA)
ENST00000468823.1:n.577G>T (GLA)
ENST00000493905.6:c.*199G>T (GLA)	ENSP00000476935.1:n.*199G>T
NM_000169.2:c.811G>T , LRG_672t1:c.811G>T (GLA)	NP_000160.1:p.Gly271Cys
NM_001199973.1:c.408+3101C>A (RPL36A-HNRNPH2)	NP_001186902.1:n.408+3101C>A
NM_001199974.1:c.285+6736C>A (RPL36A-HNRNPH2)	NP_001186903.1:n.285+6736C>A
XR_938397.1:n.896G>T (GLA)
XR_938397.2:n.917G>T (GLA)
NM_001199973.2:c.300+3101C>A (RPL36A-HNRNPH2)	NP_001186902.2:n.300+3101C>A
NM_001199974.2:c.177+6736C>A (RPL36A-HNRNPH2)	NP_001186903.2:n.177+6736C>A
NM_000169.3:c.811G>T (GLA) MANE Select	NP_000160.1:p.Gly271Cys
NR_164783.1:n.890G>T (GLA)