Canonical Allele Identifier: CA413921259

Gene: GLA RPL36A-HNRNPH2

Linked Data

• MyVariant Identifiers: chrX:g.100653088C>A (hg19) ; chrX:g.101398100C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.101398100C>A , CM000685.2:g.101398100C>A	GRCh38
NC_000023.10:g.100653088C>A , CM000685.1:g.100653088C>A	GRCh37
NC_000023.9:g.100539744C>A	NCBI36
NG_007119.1:g.14864G>T , LRG_672:g.14864G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000486121.7:c.*446-1G>T (GLA)	ENSP00000501124.2:n.*446-1G>T
ENST00000674127.2:c.*503-1G>T (GLA)	ENSP00000501044.2:n.*503-1G>T
ENST00000710365.1:c.1075-1G>T (GLA)	ENSP00000518234.1:n.1075-1G>T
ENST00000218516.4:c.1000-1G>T (GLA) MANE Select	ENSP00000218516.4:n.1000-1G>T
ENST00000466414.2:n.1136-1G>T (GLA)
ENST00000468823.2:n.2421G>T (GLA)
ENST00000479445.2:n.1614-1G>T (GLA)
ENST00000480513.6:c.*308-1G>T (GLA)	ENSP00000497055.1:n.*308-1G>T
ENST00000486121.6:c.1045-1G>T (GLA)
ENST00000649178.1:c.1123-1G>T (GLA)	ENSP00000498186.1:n.1123-1G>T
ENST00000674127.1:c.1100-1G>T (GLA)	ENSP00000501044.1:n.1100-1G>T
ENST00000674142.1:n.1304-1G>T (GLA)
ENST00000675592.1:c.802-1G>T (GLA)	ENSP00000502239.1:n.802-1G>T
ENST00000675799.1:c.*525-1G>T (GLA)	ENSP00000502661.1:n.*525-1G>T
ENST00000675968.1:n.3871-1G>T (GLA)
ENST00000676156.1:c.964-1G>T (GLA)	ENSP00000501730.1:n.964-1G>T
ENST00000676372.1:c.1066-1G>T (GLA)	ENSP00000502805.1:n.1066-1G>T
ENST00000218516.3:c.1000-1G>T (GLA)	ENSP00000218516.3:n.1000-1G>T
ENST00000409170.3:c.300+2643C>A (RPL36A-HNRNPH2)	ENSP00000386655.4:n.300+2643C>A
ENST00000409338.5:c.177+6278C>A (RPL36A-HNRNPH2)	ENSP00000386974.2:n.177+6278C>A
ENST00000466414.1:n.326-1G>T (GLA)
ENST00000493905.6:c.*388-1G>T (GLA)	ENSP00000476935.1:n.*388-1G>T
NM_000169.2:c.1000-1G>T , LRG_672t1:c.1000-1G>T (GLA)	NP_000160.1:n.1000-1G>T
NM_001199973.1:c.408+2643C>A (RPL36A-HNRNPH2)	NP_001186902.1:n.408+2643C>A
NM_001199974.1:c.285+6278C>A (RPL36A-HNRNPH2)	NP_001186903.1:n.285+6278C>A
XR_938397.1:n.1085-1G>T (GLA)
XR_938397.2:n.1106-1G>T (GLA)
NM_001199973.2:c.300+2643C>A (RPL36A-HNRNPH2)	NP_001186902.2:n.300+2643C>A
NM_001199974.2:c.177+6278C>A (RPL36A-HNRNPH2)	NP_001186903.2:n.177+6278C>A
NM_000169.3:c.1000-1G>T (GLA) MANE Select	NP_000160.1:n.1000-1G>T
NR_164783.1:n.1079-1G>T (GLA)