Canonical Allele Identifier: CA413930582

Gene: GLA RPL36A-HNRNPH2

Linked Data

• MyVariant Identifiers: chrX:g.100656764C>T (hg19) ; chrX:g.101401776C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.101401776C>T , CM000685.2:g.101401776C>T	GRCh38
NC_000023.10:g.100656764C>T , CM000685.1:g.100656764C>T	GRCh37
NC_000023.9:g.100543420C>T	NCBI36
NG_007119.1:g.11188G>A , LRG_672:g.11188G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000486121.7:c.403G>A (GLA)	ENSP00000501124.2:p.Ala135Thr
ENST00000674127.2:c.403G>A (GLA)	ENSP00000501044.2:p.Ala135Thr
ENST00000710365.1:c.478G>A (GLA)	ENSP00000518234.1:p.Ala160Thr
ENST00000218516.4:c.403G>A (GLA) MANE Select	ENSP00000218516.4:p.Ala135Thr
ENST00000466414.2:n.322G>A (GLA)
ENST00000468823.2:n.464G>A (GLA)
ENST00000479445.2:n.401G>A (GLA)
ENST00000480513.6:c.403G>A (GLA)	ENSP00000497055.1:p.Ala135Thr
ENST00000486121.6:c.333G>A (GLA)
ENST00000649178.1:c.526G>A (GLA)	ENSP00000498186.1:p.Ala176Thr
ENST00000674127.1:c.331G>A (GLA)	ENSP00000501044.1:p.Ala111Thr
ENST00000674142.1:n.490G>A (GLA)
ENST00000674634.2:c.403G>A (GLA)	ENSP00000502629.2:p.Ala135Thr
ENST00000675592.1:c.403G>A (GLA)	ENSP00000502239.1:p.Ala135Thr
ENST00000675799.1:c.403G>A (GLA)	ENSP00000502661.1:p.Ala135Thr
ENST00000675968.1:n.464G>A (GLA)
ENST00000676156.1:c.403G>A (GLA)	ENSP00000501730.1:p.Ala135Thr
ENST00000676372.1:c.403G>A (GLA)	ENSP00000502805.1:p.Ala135Thr
ENST00000218516.3:c.403G>A (GLA)	ENSP00000218516.3:p.Ala135Thr
ENST00000409170.3:c.300+6319C>T (RPL36A-HNRNPH2)	ENSP00000386655.4:n.300+6319C>T
ENST00000409338.5:c.177+9954C>T (RPL36A-HNRNPH2)	ENSP00000386974.2:n.177+9954C>T
ENST00000479445.1:n.387G>A (GLA)
ENST00000480513.5:n.333G>A (GLA)
ENST00000486121.5:n.333G>A (GLA)
ENST00000493905.6:c.403G>A (GLA)	ENSP00000476935.1:p.Ala135Thr
NM_000169.2:c.403G>A , LRG_672t1:c.403G>A (GLA)	NP_000160.1:p.Ala135Thr
NM_001199973.1:c.408+6319C>T (RPL36A-HNRNPH2)	NP_001186902.1:n.408+6319C>T
NM_001199974.1:c.285+9954C>T (RPL36A-HNRNPH2)	NP_001186903.1:n.285+9954C>T
XR_938397.1:n.431G>A (GLA)
XR_938397.2:n.452G>A (GLA)
NM_001199973.2:c.300+6319C>T (RPL36A-HNRNPH2)	NP_001186902.2:n.300+6319C>T
NM_001199974.2:c.177+9954C>T (RPL36A-HNRNPH2)	NP_001186903.2:n.177+9954C>T
NM_000169.3:c.403G>A (GLA) MANE Select	NP_000160.1:p.Ala135Thr
NR_164783.1:n.425G>A (GLA)