Canonical Allele Identifier: CA517525944

Gene: GLA RPL36A-HNRNPH2

Linked Data

• MyVariant Identifiers: chrX:g.100662837G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.101407849G>A , CM000685.2:g.101407849G>A	GRCh38
NC_000023.10:g.100662837G>A , CM000685.1:g.100662837G>A	GRCh37
NC_000023.9:g.100549493G>A	NCBI36
NG_007119.1:g.5115C>T , LRG_672:g.5115C>T
NG_016327.1:g.4647G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000486121.7:c.55C>T (GLA)	ENSP00000501124.2:p.Leu19=
ENST00000674127.2:c.55C>T (GLA)	ENSP00000501044.2:p.Leu19=
ENST00000710365.1:c.55C>T (GLA)	ENSP00000518234.1:p.Leu19=
ENST00000218516.4:c.55C>T (GLA) MANE Select	ENSP00000218516.4:p.Leu19=
ENST00000468823.2:n.116C>T (GLA)
ENST00000479445.2:n.53C>T (GLA)
ENST00000480513.6:c.55C>T (GLA)	ENSP00000497055.1:p.Leu19=
ENST00000649178.1:c.55C>T (GLA)	ENSP00000498186.1:p.Leu19=
ENST00000674142.1:n.142C>T (GLA)
ENST00000674634.2:c.55C>T (GLA)	ENSP00000502629.2:p.Leu19=
ENST00000675592.1:c.55C>T (GLA)	ENSP00000502239.1:p.Leu19=
ENST00000675799.1:c.55C>T (GLA)	ENSP00000502661.1:p.Leu19=
ENST00000675968.1:n.116C>T (GLA)
ENST00000676156.1:c.55C>T (GLA)	ENSP00000501730.1:p.Leu19=
ENST00000676372.1:c.55C>T (GLA)	ENSP00000502805.1:p.Leu19=
ENST00000218516.3:c.55C>T (GLA)	ENSP00000218516.3:p.Leu19=
ENST00000409170.3:c.301-4087G>A (RPL36A-HNRNPH2)	ENSP00000386655.4:n.301-4087G>A
ENST00000409338.5:c.178-4087G>A (RPL36A-HNRNPH2)	ENSP00000386974.2:n.178-4087G>A
ENST00000479445.1:n.39C>T (GLA)
ENST00000493905.6:c.55C>T (GLA)	ENSP00000476935.1:p.Leu19=
NM_000169.2:c.55C>T , LRG_672t1:c.55C>T (GLA)	NP_000160.1:p.Leu19=
NM_001199973.1:c.409-4087G>A (RPL36A-HNRNPH2)	NP_001186902.1:n.409-4087G>A
NM_001199974.1:c.286-4087G>A (RPL36A-HNRNPH2)	NP_001186903.1:n.286-4087G>A
XR_938397.1:n.83C>T (GLA)
XR_938397.2:n.104C>T (GLA)
NM_001199973.2:c.301-4087G>A (RPL36A-HNRNPH2)	NP_001186902.2:n.301-4087G>A
NM_001199974.2:c.178-4087G>A (RPL36A-HNRNPH2)	NP_001186903.2:n.178-4087G>A
NM_000169.3:c.55C>T (GLA) MANE Select	NP_000160.1:p.Leu19=
NR_164783.1:n.77C>T (GLA)