Canonical Allele Identifier: CA352666

Gene: GLA RPL36A-HNRNPH2

Linked Data

• ClinVar Variation Id: 1324470
• ClinVar RCV Id: RCV001782190 ; RCV002034593
• dbSNP Id: rs869312226
• COSMIC: COSM1111874
• MyVariant Identifiers: chrX:g.100662783C>T (hg19) ; chrX:g.101407795C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.101407795C>T , CM000685.2:g.101407795C>T	GRCh38
NC_000023.10:g.100662783C>T , CM000685.1:g.100662783C>T	GRCh37
NC_000023.9:g.100549439C>T	NCBI36
NG_007119.1:g.5169G>A , LRG_672:g.5169G>A
NG_016327.1:g.4593C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000486121.7:c.109G>A (GLA)	ENSP00000501124.2:p.Ala37Thr
ENST00000674127.2:c.109G>A (GLA)	ENSP00000501044.2:p.Ala37Thr
ENST00000710365.1:c.109G>A (GLA)	ENSP00000518234.1:p.Ala37Thr
ENST00000218516.4:c.109G>A (GLA) MANE Select	ENSP00000218516.4:p.Ala37Thr
ENST00000466414.2:n.28G>A (GLA)
ENST00000468823.2:n.170G>A (GLA)
ENST00000479445.2:n.107G>A (GLA)
ENST00000480513.6:c.109G>A (GLA)	ENSP00000497055.1:p.Ala37Thr
ENST00000486121.6:c.39G>A (GLA)
ENST00000649178.1:c.109G>A (GLA)	ENSP00000498186.1:p.Ala37Thr
ENST00000674127.1:c.37G>A (GLA)	ENSP00000501044.1:p.Ala13Thr
ENST00000674142.1:n.196G>A (GLA)
ENST00000674634.2:c.109G>A (GLA)	ENSP00000502629.2:p.Ala37Thr
ENST00000675592.1:c.109G>A (GLA)	ENSP00000502239.1:p.Ala37Thr
ENST00000675799.1:c.109G>A (GLA)	ENSP00000502661.1:p.Ala37Thr
ENST00000675968.1:n.170G>A (GLA)
ENST00000676156.1:c.109G>A (GLA)	ENSP00000501730.1:p.Ala37Thr
ENST00000676372.1:c.109G>A (GLA)	ENSP00000502805.1:p.Ala37Thr
ENST00000218516.3:c.109G>A (GLA)	ENSP00000218516.3:p.Ala37Thr
ENST00000409170.3:c.301-4141C>T (RPL36A-HNRNPH2)	ENSP00000386655.4:n.301-4141C>T
ENST00000409338.5:c.178-4141C>T (RPL36A-HNRNPH2)	ENSP00000386974.2:n.178-4141C>T
ENST00000479445.1:n.93G>A (GLA)
ENST00000480513.5:n.39G>A (GLA)
ENST00000486121.5:n.39G>A (GLA)
ENST00000493905.6:c.109G>A (GLA)	ENSP00000476935.1:p.Ala37Thr
NM_000169.2:c.109G>A , LRG_672t1:c.109G>A (GLA)	NP_000160.1:p.Ala37Thr
NM_001199973.1:c.409-4141C>T (RPL36A-HNRNPH2)	NP_001186902.1:n.409-4141C>T
NM_001199974.1:c.286-4141C>T (RPL36A-HNRNPH2)	NP_001186903.1:n.286-4141C>T
XR_938397.1:n.137G>A (GLA)
XR_938397.2:n.158G>A (GLA)
NM_001199973.2:c.301-4141C>T (RPL36A-HNRNPH2)	NP_001186902.2:n.301-4141C>T
NM_001199974.2:c.178-4141C>T (RPL36A-HNRNPH2)	NP_001186903.2:n.178-4141C>T
NM_000169.3:c.109G>A (GLA) MANE Select	NP_000160.1:p.Ala37Thr
NR_164783.1:n.131G>A (GLA)