Canonical Allele Identifier: CA2448297754
Gene: GLA HGNC NCBI
RPL36A-HNRNPH2 HGNC NCBI

Linked Data

dbSNP Id: rs1928106776

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101397723A>C , CM000685.2:g.101397723A>C GRCh38
NC_000023.10:g.100652711A>C , CM000685.1:g.100652711A>C GRCh37
NC_000023.9:g.100539367A>C NCBI36
NG_007119.1:g.15241T>G , LRG_672:g.15241T>G
NG_012523.1:g.11764A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000710365.1:c.*86T>G (GLA) ENSP00000518234.1:n.*86T>G
ENST00000468823.2:n.2798T>G (GLA)
ENST00000674142.1:n.1421+259T>G (GLA)
ENST00000409170.3:c.300+2266A>C (RPL36A-HNRNPH2) ENSP00000386655.4:n.300+2266A>C
ENST00000409338.5:c.177+5901A>C (RPL36A-HNRNPH2) ENSP00000386974.2:n.177+5901A>C
NM_001199973.1:c.408+2266A>C (RPL36A-HNRNPH2) NP_001186902.1:n.408+2266A>C
NM_001199974.1:c.285+5901A>C (RPL36A-HNRNPH2) NP_001186903.1:n.285+5901A>C
NM_001199973.2:c.300+2266A>C (RPL36A-HNRNPH2) NP_001186902.2:n.300+2266A>C
NM_001199974.2:c.177+5901A>C (RPL36A-HNRNPH2) NP_001186903.2:n.177+5901A>C