Canonical Allele Identifier: CA869301895
Gene: GLA HGNC NCBI
RPL36A-HNRNPH2 HGNC NCBI

Linked Data

dbSNP Id: rs1469853479
MyVariant Identifiers: chrX:g.101397732C>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101397732C>T , CM000685.2:g.101397732C>T GRCh38
NC_000023.10:g.100652720C>T , CM000685.1:g.100652720C>T GRCh37
NC_000023.9:g.100539376C>T NCBI36
NG_007119.1:g.15232G>A , LRG_672:g.15232G>A
NG_012523.1:g.11773C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000710365.1:c.*77G>A (GLA) ENSP00000518234.1:n.*77G>A
ENST00000468823.2:n.2789G>A (GLA)
ENST00000674142.1:n.1421+250G>A (GLA)
ENST00000409170.3:c.300+2275C>T (RPL36A-HNRNPH2) ENSP00000386655.4:n.300+2275C>T
ENST00000409338.5:c.177+5910C>T (RPL36A-HNRNPH2) ENSP00000386974.2:n.177+5910C>T
NM_001199973.1:c.408+2275C>T (RPL36A-HNRNPH2) NP_001186902.1:n.408+2275C>T
NM_001199974.1:c.285+5910C>T (RPL36A-HNRNPH2) NP_001186903.1:n.285+5910C>T
NM_001199973.2:c.300+2275C>T (RPL36A-HNRNPH2) NP_001186902.2:n.300+2275C>T
NM_001199974.2:c.177+5910C>T (RPL36A-HNRNPH2) NP_001186903.2:n.177+5910C>T