Canonical Allele Identifier: CA517525684

Gene: GLA RPL36A-HNRNPH2

Linked Data

• MyVariant Identifiers: chrX:g.100662778C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.101407790C>T , CM000685.2:g.101407790C>T	GRCh38
NC_000023.10:g.100662778C>T , CM000685.1:g.100662778C>T	GRCh37
NC_000023.9:g.100549434C>T	NCBI36
NG_007119.1:g.5174G>A , LRG_672:g.5174G>A
NG_016327.1:g.4588C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000486121.7:c.114G>A (GLA)	ENSP00000501124.2:p.Arg38=
ENST00000674127.2:c.114G>A (GLA)	ENSP00000501044.2:p.Arg38=
ENST00000710365.1:c.114G>A (GLA)	ENSP00000518234.1:p.Arg38=
ENST00000218516.4:c.114G>A (GLA) MANE Select	ENSP00000218516.4:p.Arg38=
ENST00000466414.2:n.33G>A (GLA)
ENST00000468823.2:n.175G>A (GLA)
ENST00000479445.2:n.112G>A (GLA)
ENST00000480513.6:c.114G>A (GLA)	ENSP00000497055.1:p.Arg38=
ENST00000486121.6:c.44G>A (GLA)
ENST00000649178.1:c.114G>A (GLA)	ENSP00000498186.1:p.Arg38=
ENST00000674127.1:c.42G>A (GLA)	ENSP00000501044.1:p.Arg14=
ENST00000674142.1:n.201G>A (GLA)
ENST00000674634.2:c.114G>A (GLA)	ENSP00000502629.2:p.Arg38=
ENST00000675592.1:c.114G>A (GLA)	ENSP00000502239.1:p.Arg38=
ENST00000675799.1:c.114G>A (GLA)	ENSP00000502661.1:p.Arg38=
ENST00000675968.1:n.175G>A (GLA)
ENST00000676156.1:c.114G>A (GLA)	ENSP00000501730.1:p.Arg38=
ENST00000676372.1:c.114G>A (GLA)	ENSP00000502805.1:p.Arg38=
ENST00000218516.3:c.114G>A (GLA)	ENSP00000218516.3:p.Arg38=
ENST00000409170.3:c.301-4146C>T (RPL36A-HNRNPH2)	ENSP00000386655.4:n.301-4146C>T
ENST00000409338.5:c.178-4146C>T (RPL36A-HNRNPH2)	ENSP00000386974.2:n.178-4146C>T
ENST00000479445.1:n.98G>A (GLA)
ENST00000480513.5:n.44G>A (GLA)
ENST00000486121.5:n.44G>A (GLA)
ENST00000493905.6:c.114G>A (GLA)	ENSP00000476935.1:p.Arg38=
NM_000169.2:c.114G>A , LRG_672t1:c.114G>A (GLA)	NP_000160.1:p.Arg38=
NM_001199973.1:c.409-4146C>T (RPL36A-HNRNPH2)	NP_001186902.1:n.409-4146C>T
NM_001199974.1:c.286-4146C>T (RPL36A-HNRNPH2)	NP_001186903.1:n.286-4146C>T
XR_938397.1:n.142G>A (GLA)
XR_938397.2:n.163G>A (GLA)
NM_001199973.2:c.301-4146C>T (RPL36A-HNRNPH2)	NP_001186902.2:n.301-4146C>T
NM_001199974.2:c.178-4146C>T (RPL36A-HNRNPH2)	NP_001186903.2:n.178-4146C>T
NM_000169.3:c.114G>A (GLA) MANE Select	NP_000160.1:p.Arg38=
NR_164783.1:n.136G>A (GLA)