Canonical Allele Identifier: CA413921115

Gene: GLA RPL36A-HNRNPH2

Linked Data

• MyVariant Identifiers: chrX:g.100653045C>T (hg19) ; chrX:g.101398057C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.101398057C>T , CM000685.2:g.101398057C>T	GRCh38
NC_000023.10:g.100653045C>T , CM000685.1:g.100653045C>T	GRCh37
NC_000023.9:g.100539701C>T	NCBI36
NG_007119.1:g.14907G>A , LRG_672:g.14907G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000486121.7:c.*488G>A (GLA)	ENSP00000501124.2:n.*488G>A
ENST00000674127.2:c.*545G>A (GLA)	ENSP00000501044.2:n.*545G>A
ENST00000710365.1:c.1117G>A (GLA)	ENSP00000518234.1:p.Ala373Thr
ENST00000218516.4:c.1042G>A (GLA) MANE Select	ENSP00000218516.4:p.Ala348Thr
ENST00000466414.2:n.1178G>A (GLA)
ENST00000468823.2:n.2464G>A (GLA)
ENST00000479445.2:n.1656G>A (GLA)
ENST00000480513.6:c.*350G>A (GLA)	ENSP00000497055.1:n.*350G>A
ENST00000486121.6:c.1087G>A (GLA)
ENST00000649178.1:c.1165G>A (GLA)	ENSP00000498186.1:p.Ala389Thr
ENST00000674127.1:c.1142G>A (GLA)	ENSP00000501044.1:n.1142G>A
ENST00000674142.1:n.1346G>A (GLA)
ENST00000675592.1:c.844G>A (GLA)	ENSP00000502239.1:p.Ala282Thr
ENST00000675799.1:c.*567G>A (GLA)	ENSP00000502661.1:n.*567G>A
ENST00000675968.1:n.3913G>A (GLA)
ENST00000676156.1:c.1006G>A (GLA)	ENSP00000501730.1:p.Ala336Thr
ENST00000676372.1:c.1108G>A (GLA)	ENSP00000502805.1:n.1108G>A
ENST00000218516.3:c.1042G>A (GLA)	ENSP00000218516.3:p.Ala348Thr
ENST00000409170.3:c.300+2600C>T (RPL36A-HNRNPH2)	ENSP00000386655.4:n.300+2600C>T
ENST00000409338.5:c.177+6235C>T (RPL36A-HNRNPH2)	ENSP00000386974.2:n.177+6235C>T
ENST00000466414.1:n.368G>A (GLA)
ENST00000493905.6:c.*430G>A (GLA)	ENSP00000476935.1:n.*430G>A
NM_000169.2:c.1042G>A , LRG_672t1:c.1042G>A (GLA)	NP_000160.1:p.Ala348Thr
NM_001199973.1:c.408+2600C>T (RPL36A-HNRNPH2)	NP_001186902.1:n.408+2600C>T
NM_001199974.1:c.285+6235C>T (RPL36A-HNRNPH2)	NP_001186903.1:n.285+6235C>T
XR_938397.1:n.1127G>A (GLA)
XR_938397.2:n.1148G>A (GLA)
NM_001199973.2:c.300+2600C>T (RPL36A-HNRNPH2)	NP_001186902.2:n.300+2600C>T
NM_001199974.2:c.177+6235C>T (RPL36A-HNRNPH2)	NP_001186903.2:n.177+6235C>T
NM_000169.3:c.1042G>A (GLA) MANE Select	NP_000160.1:p.Ala348Thr
NR_164783.1:n.1121G>A (GLA)