Canonical Allele Identifier: CA413920772

Gene: GLA RPL36A-HNRNPH2

Linked Data

• MyVariant Identifiers: chrX:g.100653003G>A (hg19) ; chrX:g.101398015G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.101398015G>A , CM000685.2:g.101398015G>A	GRCh38
NC_000023.10:g.100653003G>A , CM000685.1:g.100653003G>A	GRCh37
NC_000023.9:g.100539659G>A	NCBI36
NG_007119.1:g.14949C>T , LRG_672:g.14949C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000486121.7:c.*530C>T (GLA)	ENSP00000501124.2:n.*530C>T
ENST00000674127.2:c.*587C>T (GLA)	ENSP00000501044.2:n.*587C>T
ENST00000710365.1:c.1159C>T (GLA)	ENSP00000518234.1:p.Pro387Ser
ENST00000218516.4:c.1084C>T (GLA) MANE Select	ENSP00000218516.4:p.Pro362Ser
ENST00000466414.2:n.1220C>T (GLA)
ENST00000468823.2:n.2506C>T (GLA)
ENST00000479445.2:n.1698C>T (GLA)
ENST00000480513.6:c.*392C>T (GLA)	ENSP00000497055.1:n.*392C>T
ENST00000486121.6:c.1129C>T (GLA)
ENST00000649178.1:c.1207C>T (GLA)	ENSP00000498186.1:p.Pro403Ser
ENST00000674127.1:c.1184C>T (GLA)	ENSP00000501044.1:n.1184C>T
ENST00000674142.1:n.1388C>T (GLA)
ENST00000675592.1:c.886C>T (GLA)	ENSP00000502239.1:p.Pro296Ser
ENST00000675799.1:c.*609C>T (GLA)	ENSP00000502661.1:n.*609C>T
ENST00000675968.1:n.3955C>T (GLA)
ENST00000676156.1:c.1048C>T (GLA)	ENSP00000501730.1:p.Pro350Ser
ENST00000676372.1:c.1150C>T (GLA)	ENSP00000502805.1:n.1150C>T
ENST00000218516.3:c.1084C>T (GLA)	ENSP00000218516.3:p.Pro362Ser
ENST00000409170.3:c.300+2558G>A (RPL36A-HNRNPH2)	ENSP00000386655.4:n.300+2558G>A
ENST00000409338.5:c.177+6193G>A (RPL36A-HNRNPH2)	ENSP00000386974.2:n.177+6193G>A
ENST00000466414.1:n.410C>T (GLA)
ENST00000493905.6:c.*472C>T (GLA)	ENSP00000476935.1:n.*472C>T
NM_000169.2:c.1084C>T , LRG_672t1:c.1084C>T (GLA)	NP_000160.1:p.Pro362Ser
NM_001199973.1:c.408+2558G>A (RPL36A-HNRNPH2)	NP_001186902.1:n.408+2558G>A
NM_001199974.1:c.285+6193G>A (RPL36A-HNRNPH2)	NP_001186903.1:n.285+6193G>A
XR_938397.1:n.1169C>T (GLA)
XR_938397.2:n.1190C>T (GLA)
NM_001199973.2:c.300+2558G>A (RPL36A-HNRNPH2)	NP_001186902.2:n.300+2558G>A
NM_001199974.2:c.177+6193G>A (RPL36A-HNRNPH2)	NP_001186903.2:n.177+6193G>A
NM_000169.3:c.1084C>T (GLA) MANE Select	NP_000160.1:p.Pro362Ser
NR_164783.1:n.1163C>T (GLA)