Canonical Allele Identifier: CA517737047
Gene: GLA HGNC NCBI
RPL36A-HNRNPH2 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.100653797T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101398809T>A , CM000685.2:g.101398809T>A GRCh38
NC_000023.10:g.100653797T>A , CM000685.1:g.100653797T>A GRCh37
NC_000023.9:g.100540453T>A NCBI36
NG_007119.1:g.14155A>T , LRG_672:g.14155A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000486121.7:c.*223A>T (GLA) ENSP00000501124.2:n.*223A>T
ENST00000674127.2:c.*280A>T (GLA) ENSP00000501044.2:n.*280A>T
ENST00000710365.1:c.852A>T (GLA) ENSP00000518234.1:p.Pro284=
ENST00000218516.4:c.777A>T (GLA) MANE Select ENSP00000218516.4:p.Pro259=
ENST00000466414.2:n.696A>T (GLA)
ENST00000468823.2:n.1712A>T (GLA)
ENST00000479445.2:n.1174A>T (GLA)
ENST00000480513.6:c.*85A>T (GLA) ENSP00000497055.1:n.*85A>T
ENST00000486121.6:c.822A>T (GLA)
ENST00000649178.1:c.900A>T (GLA) ENSP00000498186.1:p.Pro300=
ENST00000674127.1:c.877A>T (GLA) ENSP00000501044.1:n.877A>T
ENST00000674142.1:n.864A>T (GLA)
ENST00000674634.2:c.777A>T (GLA) ENSP00000502629.2:p.Pro259=
ENST00000675592.1:c.777A>T (GLA) ENSP00000502239.1:p.Pro259=
ENST00000675799.1:c.*85A>T (GLA) ENSP00000502661.1:n.*85A>T
ENST00000675968.1:n.3431A>T (GLA)
ENST00000676156.1:c.741A>T (GLA) ENSP00000501730.1:p.Pro247=
ENST00000676372.1:c.777A>T (GLA) ENSP00000502805.1:p.Pro259=
ENST00000218516.3:c.777A>T (GLA) ENSP00000218516.3:p.Pro259=
ENST00000409170.3:c.300+3352T>A (RPL36A-HNRNPH2) ENSP00000386655.4:n.300+3352T>A
ENST00000409338.5:c.177+6987T>A (RPL36A-HNRNPH2) ENSP00000386974.2:n.177+6987T>A
ENST00000468823.1:n.326A>T (GLA)
ENST00000493905.6:c.*165A>T (GLA) ENSP00000476935.1:n.*165A>T
NM_000169.2:c.777A>T , LRG_672t1:c.777A>T (GLA) NP_000160.1:p.Pro259=
NM_001199973.1:c.408+3352T>A (RPL36A-HNRNPH2) NP_001186902.1:n.408+3352T>A
NM_001199974.1:c.285+6987T>A (RPL36A-HNRNPH2) NP_001186903.1:n.285+6987T>A
XR_938397.1:n.862A>T (GLA)
XR_938397.2:n.883A>T (GLA)
NM_001199973.2:c.300+3352T>A (RPL36A-HNRNPH2) NP_001186902.2:n.300+3352T>A
NM_001199974.2:c.177+6987T>A (RPL36A-HNRNPH2) NP_001186903.2:n.177+6987T>A
NM_000169.3:c.777A>T (GLA) MANE Select NP_000160.1:p.Pro259=
NR_164783.1:n.856A>T (GLA)