Canonical Allele Identifier: CA413930853

Gene: GLA RPL36A-HNRNPH2

Linked Data

• MyVariant Identifiers: chrX:g.100656789G>C (hg19) ; chrX:g.101401801G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.101401801G>C , CM000685.2:g.101401801G>C	GRCh38
NC_000023.10:g.100656789G>C , CM000685.1:g.100656789G>C	GRCh37
NC_000023.9:g.100543445G>C	NCBI36
NG_007119.1:g.11163C>G , LRG_672:g.11163C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000486121.7:c.378C>G (GLA)	ENSP00000501124.2:p.Ser126Arg
ENST00000674127.2:c.378C>G (GLA)	ENSP00000501044.2:p.Ser126Arg
ENST00000710365.1:c.453C>G (GLA)	ENSP00000518234.1:p.Ser151Arg
ENST00000218516.4:c.378C>G (GLA) MANE Select	ENSP00000218516.4:p.Ser126Arg
ENST00000466414.2:n.297C>G (GLA)
ENST00000468823.2:n.439C>G (GLA)
ENST00000479445.2:n.376C>G (GLA)
ENST00000480513.6:c.378C>G (GLA)	ENSP00000497055.1:p.Ser126Arg
ENST00000486121.6:c.308C>G (GLA)
ENST00000649178.1:c.501C>G (GLA)	ENSP00000498186.1:p.Ser167Arg
ENST00000674127.1:c.306C>G (GLA)	ENSP00000501044.1:p.Ser102Arg
ENST00000674142.1:n.465C>G (GLA)
ENST00000674634.2:c.378C>G (GLA)	ENSP00000502629.2:p.Ser126Arg
ENST00000675592.1:c.378C>G (GLA)	ENSP00000502239.1:p.Ser126Arg
ENST00000675799.1:c.378C>G (GLA)	ENSP00000502661.1:p.Ser126Arg
ENST00000675968.1:n.439C>G (GLA)
ENST00000676156.1:c.378C>G (GLA)	ENSP00000501730.1:p.Ser126Arg
ENST00000676372.1:c.378C>G (GLA)	ENSP00000502805.1:p.Ser126Arg
ENST00000218516.3:c.378C>G (GLA)	ENSP00000218516.3:p.Ser126Arg
ENST00000409170.3:c.300+6344G>C (RPL36A-HNRNPH2)	ENSP00000386655.4:n.300+6344G>C
ENST00000409338.5:c.177+9979G>C (RPL36A-HNRNPH2)	ENSP00000386974.2:n.177+9979G>C
ENST00000479445.1:n.362C>G (GLA)
ENST00000480513.5:n.308C>G (GLA)
ENST00000486121.5:n.308C>G (GLA)
ENST00000493905.6:c.378C>G (GLA)	ENSP00000476935.1:p.Ser126Arg
NM_000169.2:c.378C>G , LRG_672t1:c.378C>G (GLA)	NP_000160.1:p.Ser126Arg
NM_001199973.1:c.408+6344G>C (RPL36A-HNRNPH2)	NP_001186902.1:n.408+6344G>C
NM_001199974.1:c.285+9979G>C (RPL36A-HNRNPH2)	NP_001186903.1:n.285+9979G>C
XR_938397.1:n.406C>G (GLA)
XR_938397.2:n.427C>G (GLA)
NM_001199973.2:c.300+6344G>C (RPL36A-HNRNPH2)	NP_001186902.2:n.300+6344G>C
NM_001199974.2:c.177+9979G>C (RPL36A-HNRNPH2)	NP_001186903.2:n.177+9979G>C
NM_000169.3:c.378C>G (GLA) MANE Select	NP_000160.1:p.Ser126Arg
NR_164783.1:n.400C>G (GLA)