Canonical Allele Identifier: CA413930772

Gene: GLA RPL36A-HNRNPH2

Linked Data

• ClinVar Variation Id: 2844176
• ClinVar RCV Id: RCV003623115
• MyVariant Identifiers: chrX:g.100656782G>T (hg19) ; chrX:g.101401794G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.101401794G>T , CM000685.2:g.101401794G>T	GRCh38
NC_000023.10:g.100656782G>T , CM000685.1:g.100656782G>T	GRCh37
NC_000023.9:g.100543438G>T	NCBI36
NG_007119.1:g.11170C>A , LRG_672:g.11170C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000486121.7:c.385C>A (GLA)	ENSP00000501124.2:p.Leu129Met
ENST00000674127.2:c.385C>A (GLA)	ENSP00000501044.2:p.Leu129Met
ENST00000710365.1:c.460C>A (GLA)	ENSP00000518234.1:p.Leu154Met
ENST00000218516.4:c.385C>A (GLA) MANE Select	ENSP00000218516.4:p.Leu129Met
ENST00000466414.2:n.304C>A (GLA)
ENST00000468823.2:n.446C>A (GLA)
ENST00000479445.2:n.383C>A (GLA)
ENST00000480513.6:c.385C>A (GLA)	ENSP00000497055.1:p.Leu129Met
ENST00000486121.6:c.315C>A (GLA)
ENST00000649178.1:c.508C>A (GLA)	ENSP00000498186.1:p.Leu170Met
ENST00000674127.1:c.313C>A (GLA)	ENSP00000501044.1:p.Leu105Met
ENST00000674142.1:n.472C>A (GLA)
ENST00000674634.2:c.385C>A (GLA)	ENSP00000502629.2:p.Leu129Met
ENST00000675592.1:c.385C>A (GLA)	ENSP00000502239.1:p.Leu129Met
ENST00000675799.1:c.385C>A (GLA)	ENSP00000502661.1:p.Leu129Met
ENST00000675968.1:n.446C>A (GLA)
ENST00000676156.1:c.385C>A (GLA)	ENSP00000501730.1:p.Leu129Met
ENST00000676372.1:c.385C>A (GLA)	ENSP00000502805.1:p.Leu129Met
ENST00000218516.3:c.385C>A (GLA)	ENSP00000218516.3:p.Leu129Met
ENST00000409170.3:c.300+6337G>T (RPL36A-HNRNPH2)	ENSP00000386655.4:n.300+6337G>T
ENST00000409338.5:c.177+9972G>T (RPL36A-HNRNPH2)	ENSP00000386974.2:n.177+9972G>T
ENST00000479445.1:n.369C>A (GLA)
ENST00000480513.5:n.315C>A (GLA)
ENST00000486121.5:n.315C>A (GLA)
ENST00000493905.6:c.385C>A (GLA)	ENSP00000476935.1:p.Leu129Met
NM_000169.2:c.385C>A , LRG_672t1:c.385C>A (GLA)	NP_000160.1:p.Leu129Met
NM_001199973.1:c.408+6337G>T (RPL36A-HNRNPH2)	NP_001186902.1:n.408+6337G>T
NM_001199974.1:c.285+9972G>T (RPL36A-HNRNPH2)	NP_001186903.1:n.285+9972G>T
XR_938397.1:n.413C>A (GLA)
XR_938397.2:n.434C>A (GLA)
NM_001199973.2:c.300+6337G>T (RPL36A-HNRNPH2)	NP_001186902.2:n.300+6337G>T
NM_001199974.2:c.177+9972G>T (RPL36A-HNRNPH2)	NP_001186903.2:n.177+9972G>T
NM_000169.3:c.385C>A (GLA) MANE Select	NP_000160.1:p.Leu129Met
NR_164783.1:n.407C>A (GLA)