Canonical Allele Identifier: CA413927624

Gene: GLA RPL36A-HNRNPH2

Linked Data

• gnomAD v4: X-101400718-C-T
• MyVariant Identifiers: chrX:g.100655706C>T (hg19) ; chrX:g.101400718C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.101400718C>T , CM000685.2:g.101400718C>T	GRCh38
NC_000023.10:g.100655706C>T , CM000685.1:g.100655706C>T	GRCh37
NC_000023.9:g.100542362C>T	NCBI36
NG_007119.1:g.12246G>A , LRG_672:g.12246G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000486121.7:c.*33G>A (GLA)	ENSP00000501124.2:n.*33G>A
ENST00000674127.2:c.*33G>A (GLA)	ENSP00000501044.2:n.*33G>A
ENST00000710365.1:c.662G>A (GLA)	ENSP00000518234.1:p.Arg221Lys
ENST00000218516.4:c.587G>A (GLA) MANE Select	ENSP00000218516.4:p.Arg196Lys
ENST00000466414.2:n.506G>A (GLA)
ENST00000468823.2:n.1522G>A (GLA)
ENST00000479445.2:n.984G>A (GLA)
ENST00000480513.6:c.547+914G>A (GLA)	ENSP00000497055.1:n.547+914G>A
ENST00000486121.6:c.632G>A (GLA)
ENST00000649178.1:c.710G>A (GLA)	ENSP00000498186.1:p.Arg237Lys
ENST00000674127.1:c.630G>A (GLA)	ENSP00000501044.1:n.630G>A
ENST00000674142.1:n.674G>A (GLA)
ENST00000674634.2:c.587G>A (GLA)	ENSP00000502629.2:p.Arg196Lys
ENST00000675592.1:c.587G>A (GLA)	ENSP00000502239.1:p.Arg196Lys
ENST00000675799.1:c.547+914G>A (GLA)	ENSP00000502661.1:n.547+914G>A
ENST00000675968.1:n.1522G>A (GLA)
ENST00000676156.1:c.551G>A (GLA)	ENSP00000501730.1:p.Arg184Lys
ENST00000676372.1:c.587G>A (GLA)	ENSP00000502805.1:p.Arg196Lys
ENST00000218516.3:c.587G>A (GLA)	ENSP00000218516.3:p.Arg196Lys
ENST00000409170.3:c.300+5261C>T (RPL36A-HNRNPH2)	ENSP00000386655.4:n.300+5261C>T
ENST00000409338.5:c.177+8896C>T (RPL36A-HNRNPH2)	ENSP00000386974.2:n.177+8896C>T
ENST00000468823.1:n.136G>A (GLA)
ENST00000480513.5:n.477+914G>A (GLA)
ENST00000486121.5:n.632G>A (GLA)
ENST00000493905.6:c.587G>A (GLA)	ENSP00000476935.1:p.Arg196Lys
NM_000169.2:c.587G>A , LRG_672t1:c.587G>A (GLA)	NP_000160.1:p.Arg196Lys
NM_001199973.1:c.408+5261C>T (RPL36A-HNRNPH2)	NP_001186902.1:n.408+5261C>T
NM_001199974.1:c.285+8896C>T (RPL36A-HNRNPH2)	NP_001186903.1:n.285+8896C>T
XR_938397.1:n.615G>A (GLA)
XR_938397.2:n.636G>A (GLA)
NM_001199973.2:c.300+5261C>T (RPL36A-HNRNPH2)	NP_001186902.2:n.300+5261C>T
NM_001199974.2:c.177+8896C>T (RPL36A-HNRNPH2)	NP_001186903.2:n.177+8896C>T
NM_000169.3:c.587G>A (GLA) MANE Select	NP_000160.1:p.Arg196Lys
NR_164783.1:n.609G>A (GLA)