Canonical Allele Identifier: CA413932955

Gene: GLA RPL36A-HNRNPH2

Linked Data

• MyVariant Identifiers: chrX:g.100658822C>T (hg19) ; chrX:g.101403834C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.101403834C>T , CM000685.2:g.101403834C>T	GRCh38
NC_000023.10:g.100658822C>T , CM000685.1:g.100658822C>T	GRCh37
NC_000023.9:g.100545478C>T	NCBI36
NG_007119.1:g.9130G>A , LRG_672:g.9130G>A
NG_016327.1:g.632C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000486121.7:c.346G>A (GLA)	ENSP00000501124.2:p.Gly116Arg
ENST00000674127.2:c.346G>A (GLA)	ENSP00000501044.2:p.Gly116Arg
ENST00000710365.1:c.421G>A (GLA)	ENSP00000518234.1:p.Gly141Arg
ENST00000218516.4:c.346G>A (GLA) MANE Select	ENSP00000218516.4:p.Gly116Arg
ENST00000466414.2:n.265G>A (GLA)
ENST00000468823.2:n.407G>A (GLA)
ENST00000479445.2:n.344G>A (GLA)
ENST00000480513.6:c.346G>A (GLA)	ENSP00000497055.1:p.Gly116Arg
ENST00000486121.6:c.276G>A (GLA)
ENST00000649178.1:c.469G>A (GLA)	ENSP00000498186.1:p.Gly157Arg
ENST00000674127.1:c.274G>A (GLA)	ENSP00000501044.1:p.Gly92Arg
ENST00000674142.1:n.433G>A (GLA)
ENST00000674634.2:c.346G>A (GLA)	ENSP00000502629.2:p.Gly116Arg
ENST00000675592.1:c.346G>A (GLA)	ENSP00000502239.1:p.Gly116Arg
ENST00000675799.1:c.346G>A (GLA)	ENSP00000502661.1:p.Gly116Arg
ENST00000675968.1:n.407G>A (GLA)
ENST00000676156.1:c.346G>A (GLA)	ENSP00000501730.1:p.Gly116Arg
ENST00000676372.1:c.346G>A (GLA)	ENSP00000502805.1:p.Gly116Arg
ENST00000218516.3:c.346G>A (GLA)	ENSP00000218516.3:p.Gly116Arg
ENST00000409170.3:c.301-8102C>T (RPL36A-HNRNPH2)	ENSP00000386655.4:n.301-8102C>T
ENST00000409338.5:c.178-8102C>T (RPL36A-HNRNPH2)	ENSP00000386974.2:n.178-8102C>T
ENST00000479445.1:n.330G>A (GLA)
ENST00000480513.5:n.276G>A (GLA)
ENST00000486121.5:n.276G>A (GLA)
ENST00000493905.6:c.346G>A (GLA)	ENSP00000476935.1:p.Gly116Arg
NM_000169.2:c.346G>A , LRG_672t1:c.346G>A (GLA)	NP_000160.1:p.Gly116Arg
NM_001199973.1:c.409-8102C>T (RPL36A-HNRNPH2)	NP_001186902.1:n.409-8102C>T
NM_001199974.1:c.286-8102C>T (RPL36A-HNRNPH2)	NP_001186903.1:n.286-8102C>T
XR_938397.1:n.374G>A (GLA)
XR_938397.2:n.395G>A (GLA)
NM_001199973.2:c.301-8102C>T (RPL36A-HNRNPH2)	NP_001186902.2:n.301-8102C>T
NM_001199974.2:c.178-8102C>T (RPL36A-HNRNPH2)	NP_001186903.2:n.178-8102C>T
NM_000169.3:c.346G>A (GLA) MANE Select	NP_000160.1:p.Gly116Arg
NR_164783.1:n.368G>A (GLA)