Canonical Allele Identifier: CA517737181

Gene: GLA RPL36A-HNRNPH2

Linked Data

• MyVariant Identifiers: chrX:g.100653884A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.101398896A>C , CM000685.2:g.101398896A>C	GRCh38
NC_000023.10:g.100653884A>C , CM000685.1:g.100653884A>C	GRCh37
NC_000023.9:g.100540540A>C	NCBI36
NG_007119.1:g.14068T>G , LRG_672:g.14068T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000486121.7:c.*136T>G (GLA)	ENSP00000501124.2:n.*136T>G
ENST00000674127.2:c.*193T>G (GLA)	ENSP00000501044.2:n.*193T>G
ENST00000710365.1:c.765T>G (GLA)	ENSP00000518234.1:p.Ala255=
ENST00000218516.4:c.690T>G (GLA) MANE Select	ENSP00000218516.4:p.Ala230=
ENST00000466414.2:n.609T>G (GLA)
ENST00000468823.2:n.1625T>G (GLA)
ENST00000479445.2:n.1087T>G (GLA)
ENST00000480513.6:c.598T>G (GLA)	ENSP00000497055.1:p.Ter200Gly
ENST00000486121.6:c.735T>G (GLA)
ENST00000649178.1:c.813T>G (GLA)	ENSP00000498186.1:p.Ala271=
ENST00000674127.1:c.790T>G (GLA)	ENSP00000501044.1:n.790T>G
ENST00000674142.1:n.777T>G (GLA)
ENST00000674634.2:c.690T>G (GLA)	ENSP00000502629.2:p.Ala230=
ENST00000675592.1:c.690T>G (GLA)	ENSP00000502239.1:p.Ala230=
ENST00000675799.1:c.598T>G (GLA)	ENSP00000502661.1:p.Ter200Gly
ENST00000675968.1:n.3344T>G (GLA)
ENST00000676156.1:c.654T>G (GLA)	ENSP00000501730.1:p.Ala218=
ENST00000676372.1:c.690T>G (GLA)	ENSP00000502805.1:p.Ala230=
ENST00000218516.3:c.690T>G (GLA)	ENSP00000218516.3:p.Ala230=
ENST00000409170.3:c.300+3439A>C (RPL36A-HNRNPH2)	ENSP00000386655.4:n.300+3439A>C
ENST00000409338.5:c.177+7074A>C (RPL36A-HNRNPH2)	ENSP00000386974.2:n.177+7074A>C
ENST00000468823.1:n.239T>G (GLA)
ENST00000480513.5:n.528T>G (GLA)
ENST00000493905.6:c.*78T>G (GLA)	ENSP00000476935.1:n.*78T>G
NM_000169.2:c.690T>G , LRG_672t1:c.690T>G (GLA)	NP_000160.1:p.Ala230=
NM_001199973.1:c.408+3439A>C (RPL36A-HNRNPH2)	NP_001186902.1:n.408+3439A>C
NM_001199974.1:c.285+7074A>C (RPL36A-HNRNPH2)	NP_001186903.1:n.285+7074A>C
XR_938397.1:n.775T>G (GLA)
XR_938397.2:n.796T>G (GLA)
NM_001199973.2:c.300+3439A>C (RPL36A-HNRNPH2)	NP_001186902.2:n.300+3439A>C
NM_001199974.2:c.177+7074A>C (RPL36A-HNRNPH2)	NP_001186903.2:n.177+7074A>C
NM_000169.3:c.690T>G (GLA) MANE Select	NP_000160.1:p.Ala230=
NR_164783.1:n.769T>G (GLA)