Canonical Allele Identifier: CA2448298094
Gene: GLA HGNC NCBI
RPL36A-HNRNPH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101398646A= , CM000685.2:g.101398646A= GRCh38
NC_000023.10:g.100653634A= , CM000685.1:g.100653634A= GRCh37
NC_000023.9:g.100540290A= NCBI36
NG_007119.1:g.14318T= , LRG_672:g.14318T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000486121.7:c.*248-79T= (GLA) ENSP00000501124.2:n.*248-79T=
ENST00000674127.2:c.*305-79T= (GLA) ENSP00000501044.2:n.*305-79T=
ENST00000710365.1:c.877-79T= (GLA) ENSP00000518234.1:n.877-79T=
ENST00000218516.4:c.802-79T= (GLA) MANE Select ENSP00000218516.4:n.802-79T=
ENST00000466414.2:n.859T= (GLA)
ENST00000468823.2:n.1875T= (GLA)
ENST00000479445.2:n.1337T= (GLA)
ENST00000480513.6:c.*110-79T= (GLA) ENSP00000497055.1:n.*110-79T=
ENST00000486121.6:c.847-79T= (GLA)
ENST00000649178.1:c.925-79T= (GLA) ENSP00000498186.1:n.925-79T=
ENST00000674127.1:c.902-79T= (GLA) ENSP00000501044.1:n.902-79T=
ENST00000674142.1:n.1027T= (GLA)
ENST00000674634.2:c.802-79T= (GLA) ENSP00000502629.2:n.802-79T=
ENST00000675592.1:c.801+139T= (GLA) ENSP00000502239.1:n.801+139T=
ENST00000675799.1:c.*248T= (GLA) ENSP00000502661.1:n.*248T=
ENST00000675968.1:n.3594T= (GLA)
ENST00000676156.1:c.766-79T= (GLA) ENSP00000501730.1:n.766-79T=
ENST00000676372.1:c.867+73T= (GLA) ENSP00000502805.1:n.867+73T=
ENST00000218516.3:c.802-79T= (GLA) ENSP00000218516.3:n.802-79T=
ENST00000409170.3:c.300+3189A= (RPL36A-HNRNPH2) ENSP00000386655.4:n.300+3189A=
ENST00000409338.5:c.177+6824A= (RPL36A-HNRNPH2) ENSP00000386974.2:n.177+6824A=
ENST00000466414.1:n.49T= (GLA)
ENST00000468823.1:n.489T= (GLA)
ENST00000493905.6:c.*190-79T= (GLA) ENSP00000476935.1:n.*190-79T=
NM_000169.2:c.802-79T= , LRG_672t1:c.802-79T= (GLA) NP_000160.1:n.802-79T=
NM_001199973.1:c.408+3189A= (RPL36A-HNRNPH2) NP_001186902.1:n.408+3189A=
NM_001199974.1:c.285+6824A= (RPL36A-HNRNPH2) NP_001186903.1:n.285+6824A=
XR_938397.1:n.887-79T= (GLA)
XR_938397.2:n.908-79T= (GLA)
NM_001199973.2:c.300+3189A= (RPL36A-HNRNPH2) NP_001186902.2:n.300+3189A=
NM_001199974.2:c.177+6824A= (RPL36A-HNRNPH2) NP_001186903.2:n.177+6824A=
NM_000169.3:c.802-79T= (GLA) MANE Select NP_000160.1:n.802-79T=
NR_164783.1:n.881-79T= (GLA)