Canonical Allele Identifier: CA413927172

Gene: GLA RPL36A-HNRNPH2

Linked Data

• ClinVar Variation Id: 1378123
• ClinVar RCV Id: RCV001914531
• dbSNP Id: rs2147475837
• MyVariant Identifiers: chrX:g.100655667C>G (hg19) ; chrX:g.101400679C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.101400679C>G , CM000685.2:g.101400679C>G	GRCh38
NC_000023.10:g.100655667C>G , CM000685.1:g.100655667C>G	GRCh37
NC_000023.9:g.100542323C>G	NCBI36
NG_007119.1:g.12285G>C , LRG_672:g.12285G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000486121.7:c.*72G>C (GLA)	ENSP00000501124.2:n.*72G>C
ENST00000674127.2:c.*72G>C (GLA)	ENSP00000501044.2:n.*72G>C
ENST00000710365.1:c.701G>C (GLA)	ENSP00000518234.1:p.Trp234Ser
ENST00000218516.4:c.626G>C (GLA) MANE Select	ENSP00000218516.4:p.Trp209Ser
ENST00000466414.2:n.545G>C (GLA)
ENST00000468823.2:n.1561G>C (GLA)
ENST00000479445.2:n.1023G>C (GLA)
ENST00000480513.6:c.547+953G>C (GLA)	ENSP00000497055.1:n.547+953G>C
ENST00000486121.6:c.671G>C (GLA)
ENST00000649178.1:c.749G>C (GLA)	ENSP00000498186.1:p.Trp250Ser
ENST00000674127.1:c.669G>C (GLA)	ENSP00000501044.1:n.669G>C
ENST00000674142.1:n.713G>C (GLA)
ENST00000674634.2:c.626G>C (GLA)	ENSP00000502629.2:p.Trp209Ser
ENST00000675592.1:c.626G>C (GLA)	ENSP00000502239.1:p.Trp209Ser
ENST00000675799.1:c.547+953G>C (GLA)	ENSP00000502661.1:n.547+953G>C
ENST00000675968.1:n.1561G>C (GLA)
ENST00000676156.1:c.590G>C (GLA)	ENSP00000501730.1:p.Trp197Ser
ENST00000676372.1:c.626G>C (GLA)	ENSP00000502805.1:p.Trp209Ser
ENST00000218516.3:c.626G>C (GLA)	ENSP00000218516.3:p.Trp209Ser
ENST00000409170.3:c.300+5222C>G (RPL36A-HNRNPH2)	ENSP00000386655.4:n.300+5222C>G
ENST00000409338.5:c.177+8857C>G (RPL36A-HNRNPH2)	ENSP00000386974.2:n.177+8857C>G
ENST00000468823.1:n.175G>C (GLA)
ENST00000480513.5:n.477+953G>C (GLA)
ENST00000486121.5:n.671G>C (GLA)
ENST00000493905.6:c.626G>C (GLA)	ENSP00000476935.1:p.Trp209Ser
NM_000169.2:c.626G>C , LRG_672t1:c.626G>C (GLA)	NP_000160.1:p.Trp209Ser
NM_001199973.1:c.408+5222C>G (RPL36A-HNRNPH2)	NP_001186902.1:n.408+5222C>G
NM_001199974.1:c.285+8857C>G (RPL36A-HNRNPH2)	NP_001186903.1:n.285+8857C>G
XR_938397.1:n.654G>C (GLA)
XR_938397.2:n.675G>C (GLA)
NM_001199973.2:c.300+5222C>G (RPL36A-HNRNPH2)	NP_001186902.2:n.300+5222C>G
NM_001199974.2:c.177+8857C>G (RPL36A-HNRNPH2)	NP_001186903.2:n.177+8857C>G
NM_000169.3:c.626G>C (GLA) MANE Select	NP_000160.1:p.Trp209Ser
NR_164783.1:n.648G>C (GLA)