Canonical Allele Identifier: CA413922716

Gene: GLA RPL36A-HNRNPH2

Linked Data

• ClinVar Variation Id: 496868
• ClinVar RCV Id: RCV000593774 ; RCV003509574
• dbSNP Id: rs104894839
• MyVariant Identifiers: chrX:g.100653496C>A (hg19) ; chrX:g.101398508C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.101398508C>A , CM000685.2:g.101398508C>A	GRCh38
NC_000023.10:g.100653496C>A , CM000685.1:g.100653496C>A	GRCh37
NC_000023.9:g.100540152C>A	NCBI36
NG_007119.1:g.14456G>T , LRG_672:g.14456G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000486121.7:c.*307G>T (GLA)	ENSP00000501124.2:n.*307G>T
ENST00000674127.2:c.*364G>T (GLA)	ENSP00000501044.2:n.*364G>T
ENST00000710365.1:c.936G>T (GLA)	ENSP00000518234.1:p.Trp312Cys
ENST00000218516.4:c.861G>T (GLA) MANE Select	ENSP00000218516.4:p.Trp287Cys
ENST00000466414.2:n.997G>T (GLA)
ENST00000468823.2:n.2013G>T (GLA)
ENST00000479445.2:n.1475G>T (GLA)
ENST00000480513.6:c.*169G>T (GLA)	ENSP00000497055.1:n.*169G>T
ENST00000486121.6:c.906G>T (GLA)
ENST00000649178.1:c.984G>T (GLA)	ENSP00000498186.1:p.Trp328Cys
ENST00000674127.1:c.961G>T (GLA)	ENSP00000501044.1:n.961G>T
ENST00000674142.1:n.1165G>T (GLA)
ENST00000674634.2:c.861G>T (GLA)	ENSP00000502629.2:p.Trp287Cys
ENST00000675592.1:c.801+277G>T (GLA)	ENSP00000502239.1:n.801+277G>T
ENST00000675799.1:c.*386G>T (GLA)	ENSP00000502661.1:n.*386G>T
ENST00000675968.1:n.3732G>T (GLA)
ENST00000676156.1:c.825G>T (GLA)	ENSP00000501730.1:p.Trp275Cys
ENST00000676372.1:c.927G>T (GLA)	ENSP00000502805.1:n.927G>T
ENST00000218516.3:c.861G>T (GLA)	ENSP00000218516.3:p.Trp287Cys
ENST00000409170.3:c.300+3051C>A (RPL36A-HNRNPH2)	ENSP00000386655.4:n.300+3051C>A
ENST00000409338.5:c.177+6686C>A (RPL36A-HNRNPH2)	ENSP00000386974.2:n.177+6686C>A
ENST00000466414.1:n.187G>T (GLA)
ENST00000493905.6:c.*249G>T (GLA)	ENSP00000476935.1:n.*249G>T
NM_000169.2:c.861G>T , LRG_672t1:c.861G>T (GLA)	NP_000160.1:p.Trp287Cys
NM_001199973.1:c.408+3051C>A (RPL36A-HNRNPH2)	NP_001186902.1:n.408+3051C>A
NM_001199974.1:c.285+6686C>A (RPL36A-HNRNPH2)	NP_001186903.1:n.285+6686C>A
XR_938397.1:n.946G>T (GLA)
XR_938397.2:n.967G>T (GLA)
NM_001199973.2:c.300+3051C>A (RPL36A-HNRNPH2)	NP_001186902.2:n.300+3051C>A
NM_001199974.2:c.177+6686C>A (RPL36A-HNRNPH2)	NP_001186903.2:n.177+6686C>A
NM_000169.3:c.861G>T (GLA) MANE Select	NP_000160.1:p.Trp287Cys
NR_164783.1:n.940G>T (GLA)