Canonical Allele Identifier: CA413919716

Gene: GLA RPL36A-HNRNPH2

Linked Data

• MyVariant Identifiers: chrX:g.100652901A>C (hg19) ; chrX:g.101397913A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.101397913A>C , CM000685.2:g.101397913A>C	GRCh38
NC_000023.10:g.100652901A>C , CM000685.1:g.100652901A>C	GRCh37
NC_000023.9:g.100539557A>C	NCBI36
NG_007119.1:g.15051T>G , LRG_672:g.15051T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674127.2:c.*689T>G (GLA)	ENSP00000501044.2:n.*689T>G
ENST00000710365.1:c.1261T>G (GLA)	ENSP00000518234.1:p.Phe421Val
ENST00000218516.4:c.1186T>G (GLA) MANE Select	ENSP00000218516.4:p.Phe396Val
ENST00000466414.2:n.1322T>G (GLA)
ENST00000468823.2:n.2608T>G (GLA)
ENST00000479445.2:n.1800T>G (GLA)
ENST00000649178.1:c.1309T>G (GLA)	ENSP00000498186.1:p.Phe437Val
ENST00000674127.1:c.1286T>G (GLA)	ENSP00000501044.1:n.1286T>G
ENST00000674142.1:n.1421+69T>G (GLA)
ENST00000675592.1:c.988T>G (GLA)	ENSP00000502239.1:p.Phe330Val
ENST00000675799.1:c.*711T>G (GLA)	ENSP00000502661.1:n.*711T>G
ENST00000675968.1:n.4057T>G (GLA)
ENST00000676156.1:c.1150T>G (GLA)	ENSP00000501730.1:p.Phe384Val
ENST00000676372.1:c.1252T>G (GLA)	ENSP00000502805.1:n.1252T>G
ENST00000218516.3:c.1186T>G (GLA)	ENSP00000218516.3:p.Phe396Val
ENST00000409170.3:c.300+2456A>C (RPL36A-HNRNPH2)	ENSP00000386655.4:n.300+2456A>C
ENST00000409338.5:c.177+6091A>C (RPL36A-HNRNPH2)	ENSP00000386974.2:n.177+6091A>C
ENST00000466414.1:n.512T>G (GLA)
ENST00000493905.6:c.*574T>G (GLA)	ENSP00000476935.1:n.*574T>G
NM_000169.2:c.1186T>G , LRG_672t1:c.1186T>G (GLA)	NP_000160.1:p.Phe396Val
NM_001199973.1:c.408+2456A>C (RPL36A-HNRNPH2)	NP_001186902.1:n.408+2456A>C
NM_001199974.1:c.285+6091A>C (RPL36A-HNRNPH2)	NP_001186903.1:n.285+6091A>C
XR_938397.1:n.1271T>G (GLA)
XR_938397.2:n.1292T>G (GLA)
NM_001199973.2:c.300+2456A>C (RPL36A-HNRNPH2)	NP_001186902.2:n.300+2456A>C
NM_001199974.2:c.177+6091A>C (RPL36A-HNRNPH2)	NP_001186903.2:n.177+6091A>C
NM_000169.3:c.1186T>G (GLA) MANE Select	NP_000160.1:p.Phe396Val
NR_164783.1:n.1265T>G (GLA)