Canonical Allele Identifier: CA413929122

Gene: GLA RPL36A-HNRNPH2

Linked Data

• ClinVar Variation Id: 1744116
• ClinVar RCV Id: RCV002340717
• MyVariant Identifiers: chrX:g.100656676A>G (hg19) ; chrX:g.101401688A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.101401688A>G , CM000685.2:g.101401688A>G	GRCh38
NC_000023.10:g.100656676A>G , CM000685.1:g.100656676A>G	GRCh37
NC_000023.9:g.100543332A>G	NCBI36
NG_007119.1:g.11276T>C , LRG_672:g.11276T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000486121.7:c.491T>C (GLA)	ENSP00000501124.2:p.Val164Ala
ENST00000674127.2:c.491T>C (GLA)	ENSP00000501044.2:p.Val164Ala
ENST00000710365.1:c.566T>C (GLA)	ENSP00000518234.1:p.Val189Ala
ENST00000218516.4:c.491T>C (GLA) MANE Select	ENSP00000218516.4:p.Val164Ala
ENST00000466414.2:n.410T>C (GLA)
ENST00000468823.2:n.552T>C (GLA)
ENST00000479445.2:n.489T>C (GLA)
ENST00000480513.6:c.491T>C (GLA)	ENSP00000497055.1:p.Val164Ala
ENST00000486121.6:c.421T>C (GLA)
ENST00000649178.1:c.614T>C (GLA)	ENSP00000498186.1:p.Val205Ala
ENST00000674127.1:c.419T>C (GLA)	ENSP00000501044.1:p.Val140Ala
ENST00000674142.1:n.578T>C (GLA)
ENST00000674634.2:c.491T>C (GLA)	ENSP00000502629.2:p.Val164Ala
ENST00000675592.1:c.491T>C (GLA)	ENSP00000502239.1:p.Val164Ala
ENST00000675799.1:c.491T>C (GLA)	ENSP00000502661.1:p.Val164Ala
ENST00000675968.1:n.552T>C (GLA)
ENST00000676156.1:c.491T>C (GLA)	ENSP00000501730.1:p.Val164Ala
ENST00000676372.1:c.491T>C (GLA)	ENSP00000502805.1:p.Val164Ala
ENST00000218516.3:c.491T>C (GLA)	ENSP00000218516.3:p.Val164Ala
ENST00000409170.3:c.300+6231A>G (RPL36A-HNRNPH2)	ENSP00000386655.4:n.300+6231A>G
ENST00000409338.5:c.177+9866A>G (RPL36A-HNRNPH2)	ENSP00000386974.2:n.177+9866A>G
ENST00000479445.1:n.475T>C (GLA)
ENST00000480513.5:n.421T>C (GLA)
ENST00000486121.5:n.421T>C (GLA)
ENST00000493905.6:c.491T>C (GLA)	ENSP00000476935.1:p.Val164Ala
NM_000169.2:c.491T>C , LRG_672t1:c.491T>C (GLA)	NP_000160.1:p.Val164Ala
NM_001199973.1:c.408+6231A>G (RPL36A-HNRNPH2)	NP_001186902.1:n.408+6231A>G
NM_001199974.1:c.285+9866A>G (RPL36A-HNRNPH2)	NP_001186903.1:n.285+9866A>G
XR_938397.1:n.519T>C (GLA)
XR_938397.2:n.540T>C (GLA)
NM_001199973.2:c.300+6231A>G (RPL36A-HNRNPH2)	NP_001186902.2:n.300+6231A>G
NM_001199974.2:c.177+9866A>G (RPL36A-HNRNPH2)	NP_001186903.2:n.177+9866A>G
NM_000169.3:c.491T>C (GLA) MANE Select	NP_000160.1:p.Val164Ala
NR_164783.1:n.513T>C (GLA)