Canonical Allele Identifier: CA517522919

Gene: GLA RPL36A-HNRNPH2

Linked Data

• MyVariant Identifiers: chrX:g.100656783T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.101401795T>C , CM000685.2:g.101401795T>C	GRCh38
NC_000023.10:g.100656783T>C , CM000685.1:g.100656783T>C	GRCh37
NC_000023.9:g.100543439T>C	NCBI36
NG_007119.1:g.11169A>G , LRG_672:g.11169A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000486121.7:c.384A>G (GLA)	ENSP00000501124.2:p.Gly128=
ENST00000674127.2:c.384A>G (GLA)	ENSP00000501044.2:p.Gly128=
ENST00000710365.1:c.459A>G (GLA)	ENSP00000518234.1:p.Gly153=
ENST00000218516.4:c.384A>G (GLA) MANE Select	ENSP00000218516.4:p.Gly128=
ENST00000466414.2:n.303A>G (GLA)
ENST00000468823.2:n.445A>G (GLA)
ENST00000479445.2:n.382A>G (GLA)
ENST00000480513.6:c.384A>G (GLA)	ENSP00000497055.1:p.Gly128=
ENST00000486121.6:c.314A>G (GLA)
ENST00000649178.1:c.507A>G (GLA)	ENSP00000498186.1:p.Gly169=
ENST00000674127.1:c.312A>G (GLA)	ENSP00000501044.1:p.Gly104=
ENST00000674142.1:n.471A>G (GLA)
ENST00000674634.2:c.384A>G (GLA)	ENSP00000502629.2:p.Gly128=
ENST00000675592.1:c.384A>G (GLA)	ENSP00000502239.1:p.Gly128=
ENST00000675799.1:c.384A>G (GLA)	ENSP00000502661.1:p.Gly128=
ENST00000675968.1:n.445A>G (GLA)
ENST00000676156.1:c.384A>G (GLA)	ENSP00000501730.1:p.Gly128=
ENST00000676372.1:c.384A>G (GLA)	ENSP00000502805.1:p.Gly128=
ENST00000218516.3:c.384A>G (GLA)	ENSP00000218516.3:p.Gly128=
ENST00000409170.3:c.300+6338T>C (RPL36A-HNRNPH2)	ENSP00000386655.4:n.300+6338T>C
ENST00000409338.5:c.177+9973T>C (RPL36A-HNRNPH2)	ENSP00000386974.2:n.177+9973T>C
ENST00000479445.1:n.368A>G (GLA)
ENST00000480513.5:n.314A>G (GLA)
ENST00000486121.5:n.314A>G (GLA)
ENST00000493905.6:c.384A>G (GLA)	ENSP00000476935.1:p.Gly128=
NM_000169.2:c.384A>G , LRG_672t1:c.384A>G (GLA)	NP_000160.1:p.Gly128=
NM_001199973.1:c.408+6338T>C (RPL36A-HNRNPH2)	NP_001186902.1:n.408+6338T>C
NM_001199974.1:c.285+9973T>C (RPL36A-HNRNPH2)	NP_001186903.1:n.285+9973T>C
XR_938397.1:n.412A>G (GLA)
XR_938397.2:n.433A>G (GLA)
NM_001199973.2:c.300+6338T>C (RPL36A-HNRNPH2)	NP_001186902.2:n.300+6338T>C
NM_001199974.2:c.177+9973T>C (RPL36A-HNRNPH2)	NP_001186903.2:n.177+9973T>C
NM_000169.3:c.384A>G (GLA) MANE Select	NP_000160.1:p.Gly128=
NR_164783.1:n.406A>G (GLA)