Canonical Allele Identifier: CA413930548

Gene: GLA RPL36A-HNRNPH2

Linked Data

• ClinVar Variation Id: 632837
• ClinVar RCV Id: RCV000780295
• dbSNP Id: rs1569304221
• MyVariant Identifiers: chrX:g.100656763G>A (hg19) ; chrX:g.101401775G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.101401775G>A , CM000685.2:g.101401775G>A	GRCh38
NC_000023.10:g.100656763G>A , CM000685.1:g.100656763G>A	GRCh37
NC_000023.9:g.100543419G>A	NCBI36
NG_007119.1:g.11189C>T , LRG_672:g.11189C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000486121.7:c.404C>T (GLA)	ENSP00000501124.2:p.Ala135Val
ENST00000674127.2:c.404C>T (GLA)	ENSP00000501044.2:p.Ala135Val
ENST00000710365.1:c.479C>T (GLA)	ENSP00000518234.1:p.Ala160Val
ENST00000218516.4:c.404C>T (GLA) MANE Select	ENSP00000218516.4:p.Ala135Val
ENST00000466414.2:n.323C>T (GLA)
ENST00000468823.2:n.465C>T (GLA)
ENST00000479445.2:n.402C>T (GLA)
ENST00000480513.6:c.404C>T (GLA)	ENSP00000497055.1:p.Ala135Val
ENST00000486121.6:c.334C>T (GLA)
ENST00000649178.1:c.527C>T (GLA)	ENSP00000498186.1:p.Ala176Val
ENST00000674127.1:c.332C>T (GLA)	ENSP00000501044.1:p.Ala111Val
ENST00000674142.1:n.491C>T (GLA)
ENST00000674634.2:c.404C>T (GLA)	ENSP00000502629.2:p.Ala135Val
ENST00000675592.1:c.404C>T (GLA)	ENSP00000502239.1:p.Ala135Val
ENST00000675799.1:c.404C>T (GLA)	ENSP00000502661.1:p.Ala135Val
ENST00000675968.1:n.465C>T (GLA)
ENST00000676156.1:c.404C>T (GLA)	ENSP00000501730.1:p.Ala135Val
ENST00000676372.1:c.404C>T (GLA)	ENSP00000502805.1:p.Ala135Val
ENST00000218516.3:c.404C>T (GLA)	ENSP00000218516.3:p.Ala135Val
ENST00000409170.3:c.300+6318G>A (RPL36A-HNRNPH2)	ENSP00000386655.4:n.300+6318G>A
ENST00000409338.5:c.177+9953G>A (RPL36A-HNRNPH2)	ENSP00000386974.2:n.177+9953G>A
ENST00000479445.1:n.388C>T (GLA)
ENST00000480513.5:n.334C>T (GLA)
ENST00000486121.5:n.334C>T (GLA)
ENST00000493905.6:c.404C>T (GLA)	ENSP00000476935.1:p.Ala135Val
NM_000169.2:c.404C>T , LRG_672t1:c.404C>T (GLA)	NP_000160.1:p.Ala135Val
NM_001199973.1:c.408+6318G>A (RPL36A-HNRNPH2)	NP_001186902.1:n.408+6318G>A
NM_001199974.1:c.285+9953G>A (RPL36A-HNRNPH2)	NP_001186903.1:n.285+9953G>A
XR_938397.1:n.432C>T (GLA)
XR_938397.2:n.453C>T (GLA)
NM_001199973.2:c.300+6318G>A (RPL36A-HNRNPH2)	NP_001186902.2:n.300+6318G>A
NM_001199974.2:c.177+9953G>A (RPL36A-HNRNPH2)	NP_001186903.2:n.177+9953G>A
NM_000169.3:c.404C>T (GLA) MANE Select	NP_000160.1:p.Ala135Val
NR_164783.1:n.426C>T (GLA)