Canonical Allele Identifier: CA413921513

Gene: GLA RPL36A-HNRNPH2

Linked Data

• MyVariant Identifiers: chrX:g.100653394C>G (hg19) ; chrX:g.101398406C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.101398406C>G , CM000685.2:g.101398406C>G	GRCh38
NC_000023.10:g.100653394C>G , CM000685.1:g.100653394C>G	GRCh37
NC_000023.9:g.100540050C>G	NCBI36
NG_007119.1:g.14558G>C , LRG_672:g.14558G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000486121.7:c.*409G>C (GLA)	ENSP00000501124.2:n.*409G>C
ENST00000674127.2:c.*466G>C (GLA)	ENSP00000501044.2:n.*466G>C
ENST00000710365.1:c.1038G>C (GLA)	ENSP00000518234.1:p.Gln346His
ENST00000218516.4:c.963G>C (GLA) MANE Select	ENSP00000218516.4:p.Gln321His
ENST00000466414.2:n.1099G>C (GLA)
ENST00000468823.2:n.2115G>C (GLA)
ENST00000479445.2:n.1577G>C (GLA)
ENST00000480513.6:c.*271G>C (GLA)	ENSP00000497055.1:n.*271G>C
ENST00000486121.6:c.1008G>C (GLA)
ENST00000649178.1:c.1086G>C (GLA)	ENSP00000498186.1:p.Gln362His
ENST00000674127.1:c.1063G>C (GLA)	ENSP00000501044.1:n.1063G>C
ENST00000674142.1:n.1267G>C (GLA)
ENST00000674634.2:c.963G>C (GLA)	ENSP00000502629.2:p.Gln321His
ENST00000675592.1:c.802-307G>C (GLA)	ENSP00000502239.1:n.802-307G>C
ENST00000675799.1:c.*488G>C (GLA)	ENSP00000502661.1:n.*488G>C
ENST00000675968.1:n.3834G>C (GLA)
ENST00000676156.1:c.927G>C (GLA)	ENSP00000501730.1:p.Gln309His
ENST00000676372.1:c.1029G>C (GLA)	ENSP00000502805.1:n.1029G>C
ENST00000218516.3:c.963G>C (GLA)	ENSP00000218516.3:p.Gln321His
ENST00000409170.3:c.300+2949C>G (RPL36A-HNRNPH2)	ENSP00000386655.4:n.300+2949C>G
ENST00000409338.5:c.177+6584C>G (RPL36A-HNRNPH2)	ENSP00000386974.2:n.177+6584C>G
ENST00000466414.1:n.289G>C (GLA)
ENST00000493905.6:c.*351G>C (GLA)	ENSP00000476935.1:n.*351G>C
NM_000169.2:c.963G>C , LRG_672t1:c.963G>C (GLA)	NP_000160.1:p.Gln321His
NM_001199973.1:c.408+2949C>G (RPL36A-HNRNPH2)	NP_001186902.1:n.408+2949C>G
NM_001199974.1:c.285+6584C>G (RPL36A-HNRNPH2)	NP_001186903.1:n.285+6584C>G
XR_938397.1:n.1048G>C (GLA)
XR_938397.2:n.1069G>C (GLA)
NM_001199973.2:c.300+2949C>G (RPL36A-HNRNPH2)	NP_001186902.2:n.300+2949C>G
NM_001199974.2:c.177+6584C>G (RPL36A-HNRNPH2)	NP_001186903.2:n.177+6584C>G
NM_000169.3:c.963G>C (GLA) MANE Select	NP_000160.1:p.Gln321His
NR_164783.1:n.1042G>C (GLA)