Canonical Allele Identifier: CA2580700664
Gene: GLA HGNC NCBI
RPL36A-HNRNPH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101403894T= , CM000685.2:g.101403894T= GRCh38
NC_000023.10:g.100658882T= , CM000685.1:g.100658882T= GRCh37
NC_000023.9:g.100545538T= NCBI36
NG_007119.1:g.9070A= , LRG_672:g.9070A=
NG_016327.1:g.692T=

Transcript Alleles

HGVS Amino-acid change
ENST00000486121.7:c.286A= (GLA) ENSP00000501124.2:p.Met96=
ENST00000674127.2:c.286A= (GLA) ENSP00000501044.2:p.Met96=
ENST00000710365.1:c.361A= (GLA) ENSP00000518234.1:p.Met121=
ENST00000218516.4:c.286A= (GLA) MANE Select ENSP00000218516.4:p.Met96=
ENST00000466414.2:n.205A= (GLA)
ENST00000468823.2:n.347A= (GLA)
ENST00000479445.2:n.284A= (GLA)
ENST00000480513.6:c.286A= (GLA) ENSP00000497055.1:p.Met96=
ENST00000486121.6:c.216A= (GLA)
ENST00000649178.1:c.409A= (GLA) ENSP00000498186.1:p.Met137=
ENST00000674127.1:c.214A= (GLA) ENSP00000501044.1:p.Met72=
ENST00000674142.1:n.373A= (GLA)
ENST00000674634.2:c.286A= (GLA) ENSP00000502629.2:p.Met96=
ENST00000675592.1:c.286A= (GLA) ENSP00000502239.1:p.Met96=
ENST00000675799.1:c.286A= (GLA) ENSP00000502661.1:p.Met96=
ENST00000675968.1:n.347A= (GLA)
ENST00000676156.1:c.286A= (GLA) ENSP00000501730.1:p.Met96=
ENST00000676372.1:c.286A= (GLA) ENSP00000502805.1:p.Met96=
ENST00000218516.3:c.286A= (GLA) ENSP00000218516.3:p.Met96=
ENST00000409170.3:c.301-8042T= (RPL36A-HNRNPH2) ENSP00000386655.4:n.301-8042T=
ENST00000409338.5:c.178-8042T= (RPL36A-HNRNPH2) ENSP00000386974.2:n.178-8042T=
ENST00000479445.1:n.270A= (GLA)
ENST00000480513.5:n.216A= (GLA)
ENST00000486121.5:n.216A= (GLA)
ENST00000493905.6:c.286A= (GLA) ENSP00000476935.1:p.Met96=
NM_000169.2:c.286A= , LRG_672t1:c.286A= (GLA) NP_000160.1:p.Met96=
NM_001199973.1:c.409-8042T= (RPL36A-HNRNPH2) NP_001186902.1:n.409-8042T=
NM_001199974.1:c.286-8042T= (RPL36A-HNRNPH2) NP_001186903.1:n.286-8042T=
XR_938397.1:n.314A= (GLA)
XR_938397.2:n.335A= (GLA)
NM_001199973.2:c.301-8042T= (RPL36A-HNRNPH2) NP_001186902.2:n.301-8042T=
NM_001199974.2:c.178-8042T= (RPL36A-HNRNPH2) NP_001186903.2:n.178-8042T=
NM_000169.3:c.286A= (GLA) MANE Select NP_000160.1:p.Met96=
NR_164783.1:n.308A= (GLA)