Canonical Allele Identifier: CA413919548

Gene: GLA RPL36A-HNRNPH2

Linked Data

• MyVariant Identifiers: chrX:g.100652886A>T (hg19) ; chrX:g.101397898A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.101397898A>T , CM000685.2:g.101397898A>T	GRCh38
NC_000023.10:g.100652886A>T , CM000685.1:g.100652886A>T	GRCh37
NC_000023.9:g.100539542A>T	NCBI36
NG_007119.1:g.15066T>A , LRG_672:g.15066T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674127.2:c.*704T>A (GLA)	ENSP00000501044.2:n.*704T>A
ENST00000710365.1:c.1276T>A (GLA)	ENSP00000518234.1:p.Ser426Thr
ENST00000218516.4:c.1201T>A (GLA) MANE Select	ENSP00000218516.4:p.Ser401Thr
ENST00000466414.2:n.1337T>A (GLA)
ENST00000468823.2:n.2623T>A (GLA)
ENST00000479445.2:n.1815T>A (GLA)
ENST00000649178.1:c.1324T>A (GLA)	ENSP00000498186.1:p.Ser442Thr
ENST00000674127.1:c.1301T>A (GLA)	ENSP00000501044.1:n.1301T>A
ENST00000674142.1:n.1421+84T>A (GLA)
ENST00000675592.1:c.1003T>A (GLA)	ENSP00000502239.1:p.Ser335Thr
ENST00000675799.1:c.*726T>A (GLA)	ENSP00000502661.1:n.*726T>A
ENST00000675968.1:n.4072T>A (GLA)
ENST00000676156.1:c.1165T>A (GLA)	ENSP00000501730.1:p.Ser389Thr
ENST00000676372.1:c.1267T>A (GLA)	ENSP00000502805.1:n.1267T>A
ENST00000218516.3:c.1201T>A (GLA)	ENSP00000218516.3:p.Ser401Thr
ENST00000409170.3:c.300+2441A>T (RPL36A-HNRNPH2)	ENSP00000386655.4:n.300+2441A>T
ENST00000409338.5:c.177+6076A>T (RPL36A-HNRNPH2)	ENSP00000386974.2:n.177+6076A>T
ENST00000466414.1:n.527T>A (GLA)
ENST00000493905.6:c.*589T>A (GLA)	ENSP00000476935.1:n.*589T>A
NM_000169.2:c.1201T>A , LRG_672t1:c.1201T>A (GLA)	NP_000160.1:p.Ser401Thr
NM_001199973.1:c.408+2441A>T (RPL36A-HNRNPH2)	NP_001186902.1:n.408+2441A>T
NM_001199974.1:c.285+6076A>T (RPL36A-HNRNPH2)	NP_001186903.1:n.285+6076A>T
XR_938397.1:n.1286T>A (GLA)
XR_938397.2:n.1307T>A (GLA)
NM_001199973.2:c.300+2441A>T (RPL36A-HNRNPH2)	NP_001186902.2:n.300+2441A>T
NM_001199974.2:c.177+6076A>T (RPL36A-HNRNPH2)	NP_001186903.2:n.177+6076A>T
NM_000169.3:c.1201T>A (GLA) MANE Select	NP_000160.1:p.Ser401Thr
NR_164783.1:n.1280T>A (GLA)