Canonical Allele Identifier: CA413924046

Gene: GLA RPL36A-HNRNPH2

Linked Data

• MyVariant Identifiers: chrX:g.100653805C>A (hg19) ; chrX:g.101398817C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.101398817C>A , CM000685.2:g.101398817C>A	GRCh38
NC_000023.10:g.100653805C>A , CM000685.1:g.100653805C>A	GRCh37
NC_000023.9:g.100540461C>A	NCBI36
NG_007119.1:g.14147G>T , LRG_672:g.14147G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000486121.7:c.*215G>T (GLA)	ENSP00000501124.2:n.*215G>T
ENST00000674127.2:c.*272G>T (GLA)	ENSP00000501044.2:n.*272G>T
ENST00000710365.1:c.844G>T (GLA)	ENSP00000518234.1:p.Ala282Ser
ENST00000218516.4:c.769G>T (GLA) MANE Select	ENSP00000218516.4:p.Ala257Ser
ENST00000466414.2:n.688G>T (GLA)
ENST00000468823.2:n.1704G>T (GLA)
ENST00000479445.2:n.1166G>T (GLA)
ENST00000480513.6:c.*77G>T (GLA)	ENSP00000497055.1:n.*77G>T
ENST00000486121.6:c.814G>T (GLA)
ENST00000649178.1:c.892G>T (GLA)	ENSP00000498186.1:p.Ala298Ser
ENST00000674127.1:c.869G>T (GLA)	ENSP00000501044.1:n.869G>T
ENST00000674142.1:n.856G>T (GLA)
ENST00000674634.2:c.769G>T (GLA)	ENSP00000502629.2:p.Ala257Ser
ENST00000675592.1:c.769G>T (GLA)	ENSP00000502239.1:p.Ala257Ser
ENST00000675799.1:c.*77G>T (GLA)	ENSP00000502661.1:n.*77G>T
ENST00000675968.1:n.3423G>T (GLA)
ENST00000676156.1:c.733G>T (GLA)	ENSP00000501730.1:p.Ala245Ser
ENST00000676372.1:c.769G>T (GLA)	ENSP00000502805.1:p.Ala257Ser
ENST00000218516.3:c.769G>T (GLA)	ENSP00000218516.3:p.Ala257Ser
ENST00000409170.3:c.300+3360C>A (RPL36A-HNRNPH2)	ENSP00000386655.4:n.300+3360C>A
ENST00000409338.5:c.177+6995C>A (RPL36A-HNRNPH2)	ENSP00000386974.2:n.177+6995C>A
ENST00000468823.1:n.318G>T (GLA)
ENST00000480513.5:n.607G>T (GLA)
ENST00000493905.6:c.*157G>T (GLA)	ENSP00000476935.1:n.*157G>T
NM_000169.2:c.769G>T , LRG_672t1:c.769G>T (GLA)	NP_000160.1:p.Ala257Ser
NM_001199973.1:c.408+3360C>A (RPL36A-HNRNPH2)	NP_001186902.1:n.408+3360C>A
NM_001199974.1:c.285+6995C>A (RPL36A-HNRNPH2)	NP_001186903.1:n.285+6995C>A
XR_938397.1:n.854G>T (GLA)
XR_938397.2:n.875G>T (GLA)
NM_001199973.2:c.300+3360C>A (RPL36A-HNRNPH2)	NP_001186902.2:n.300+3360C>A
NM_001199974.2:c.177+6995C>A (RPL36A-HNRNPH2)	NP_001186903.2:n.177+6995C>A
NM_000169.3:c.769G>T (GLA) MANE Select	NP_000160.1:p.Ala257Ser
NR_164783.1:n.848G>T (GLA)