Canonical Allele Identifier: CA2448299876
Gene: GLA HGNC NCBI
RPL36A-HNRNPH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101403893A= , CM000685.2:g.101403893A= GRCh38
NC_000023.10:g.100658881A= , CM000685.1:g.100658881A= GRCh37
NC_000023.9:g.100545537A= NCBI36
NG_007119.1:g.9071T= , LRG_672:g.9071T=
NG_016327.1:g.691A=

Transcript Alleles

HGVS Amino-acid change
ENST00000486121.7:c.287T= (GLA) ENSP00000501124.2:p.Met96=
ENST00000674127.2:c.287T= (GLA) ENSP00000501044.2:p.Met96=
ENST00000710365.1:c.362T= (GLA) ENSP00000518234.1:p.Met121=
ENST00000218516.4:c.287T= (GLA) MANE Select ENSP00000218516.4:p.Met96=
ENST00000466414.2:n.206T= (GLA)
ENST00000468823.2:n.348T= (GLA)
ENST00000479445.2:n.285T= (GLA)
ENST00000480513.6:c.287T= (GLA) ENSP00000497055.1:p.Met96=
ENST00000486121.6:c.217T= (GLA)
ENST00000649178.1:c.410T= (GLA) ENSP00000498186.1:p.Met137=
ENST00000674127.1:c.215T= (GLA) ENSP00000501044.1:p.Met72=
ENST00000674142.1:n.374T= (GLA)
ENST00000674634.2:c.287T= (GLA) ENSP00000502629.2:p.Met96=
ENST00000675592.1:c.287T= (GLA) ENSP00000502239.1:p.Met96=
ENST00000675799.1:c.287T= (GLA) ENSP00000502661.1:p.Met96=
ENST00000675968.1:n.348T= (GLA)
ENST00000676156.1:c.287T= (GLA) ENSP00000501730.1:p.Met96=
ENST00000676372.1:c.287T= (GLA) ENSP00000502805.1:p.Met96=
ENST00000218516.3:c.287T= (GLA) ENSP00000218516.3:p.Met96=
ENST00000409170.3:c.301-8043A= (RPL36A-HNRNPH2) ENSP00000386655.4:n.301-8043A=
ENST00000409338.5:c.178-8043A= (RPL36A-HNRNPH2) ENSP00000386974.2:n.178-8043A=
ENST00000479445.1:n.271T= (GLA)
ENST00000480513.5:n.217T= (GLA)
ENST00000486121.5:n.217T= (GLA)
ENST00000493905.6:c.287T= (GLA) ENSP00000476935.1:p.Met96=
NM_000169.2:c.287T= , LRG_672t1:c.287T= (GLA) NP_000160.1:p.Met96=
NM_001199973.1:c.409-8043A= (RPL36A-HNRNPH2) NP_001186902.1:n.409-8043A=
NM_001199974.1:c.286-8043A= (RPL36A-HNRNPH2) NP_001186903.1:n.286-8043A=
XR_938397.1:n.315T= (GLA)
XR_938397.2:n.336T= (GLA)
NM_001199973.2:c.301-8043A= (RPL36A-HNRNPH2) NP_001186902.2:n.301-8043A=
NM_001199974.2:c.178-8043A= (RPL36A-HNRNPH2) NP_001186903.2:n.178-8043A=
NM_000169.3:c.287T= (GLA) MANE Select NP_000160.1:p.Met96=
NR_164783.1:n.309T= (GLA)