Canonical Allele Identifier: CA413921223

Gene: GLA RPL36A-HNRNPH2

Linked Data

• MyVariant Identifiers: chrX:g.100653073T>G (hg19) ; chrX:g.101398085T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.101398085T>G , CM000685.2:g.101398085T>G	GRCh38
NC_000023.10:g.100653073T>G , CM000685.1:g.100653073T>G	GRCh37
NC_000023.9:g.100539729T>G	NCBI36
NG_007119.1:g.14879A>C , LRG_672:g.14879A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000486121.7:c.*460A>C (GLA)	ENSP00000501124.2:n.*460A>C
ENST00000674127.2:c.*517A>C (GLA)	ENSP00000501044.2:n.*517A>C
ENST00000710365.1:c.1089A>C (GLA)	ENSP00000518234.1:p.Glu363Asp
ENST00000218516.4:c.1014A>C (GLA) MANE Select	ENSP00000218516.4:p.Glu338Asp
ENST00000466414.2:n.1150A>C (GLA)
ENST00000468823.2:n.2436A>C (GLA)
ENST00000479445.2:n.1628A>C (GLA)
ENST00000480513.6:c.*322A>C (GLA)	ENSP00000497055.1:n.*322A>C
ENST00000486121.6:c.1059A>C (GLA)
ENST00000649178.1:c.1137A>C (GLA)	ENSP00000498186.1:p.Glu379Asp
ENST00000674127.1:c.1114A>C (GLA)	ENSP00000501044.1:n.1114A>C
ENST00000674142.1:n.1318A>C (GLA)
ENST00000675592.1:c.816A>C (GLA)	ENSP00000502239.1:p.Glu272Asp
ENST00000675799.1:c.*539A>C (GLA)	ENSP00000502661.1:n.*539A>C
ENST00000675968.1:n.3885A>C (GLA)
ENST00000676156.1:c.978A>C (GLA)	ENSP00000501730.1:p.Glu326Asp
ENST00000676372.1:c.1080A>C (GLA)	ENSP00000502805.1:n.1080A>C
ENST00000218516.3:c.1014A>C (GLA)	ENSP00000218516.3:p.Glu338Asp
ENST00000409170.3:c.300+2628T>G (RPL36A-HNRNPH2)	ENSP00000386655.4:n.300+2628T>G
ENST00000409338.5:c.177+6263T>G (RPL36A-HNRNPH2)	ENSP00000386974.2:n.177+6263T>G
ENST00000466414.1:n.340A>C (GLA)
ENST00000493905.6:c.*402A>C (GLA)	ENSP00000476935.1:n.*402A>C
NM_000169.2:c.1014A>C , LRG_672t1:c.1014A>C (GLA)	NP_000160.1:p.Glu338Asp
NM_001199973.1:c.408+2628T>G (RPL36A-HNRNPH2)	NP_001186902.1:n.408+2628T>G
NM_001199974.1:c.285+6263T>G (RPL36A-HNRNPH2)	NP_001186903.1:n.285+6263T>G
XR_938397.1:n.1099A>C (GLA)
XR_938397.2:n.1120A>C (GLA)
NM_001199973.2:c.300+2628T>G (RPL36A-HNRNPH2)	NP_001186902.2:n.300+2628T>G
NM_001199974.2:c.177+6263T>G (RPL36A-HNRNPH2)	NP_001186903.2:n.177+6263T>G
NM_000169.3:c.1014A>C (GLA) MANE Select	NP_000160.1:p.Glu338Asp
NR_164783.1:n.1093A>C (GLA)