Canonical Allele Identifier: CA2448297930
Gene: GLA HGNC NCBI
RPL36A-HNRNPH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101398324G= , CM000685.2:g.101398324G= GRCh38
NC_000023.10:g.100653312G= , CM000685.1:g.100653312G= GRCh37
NC_000023.9:g.100539968G= NCBI36
NG_007119.1:g.14640C= , LRG_672:g.14640C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000486121.7:c.*445+46C= (GLA) ENSP00000501124.2:n.*445+46C=
ENST00000674127.2:c.*502+46C= (GLA) ENSP00000501044.2:n.*502+46C=
ENST00000710365.1:c.1074+46C= (GLA) ENSP00000518234.1:n.1074+46C=
ENST00000218516.4:c.999+46C= (GLA) MANE Select ENSP00000218516.4:n.999+46C=
ENST00000466414.2:n.1135+46C= (GLA)
ENST00000468823.2:n.2197C= (GLA)
ENST00000479445.2:n.1613+46C= (GLA)
ENST00000480513.6:c.*307+46C= (GLA) ENSP00000497055.1:n.*307+46C=
ENST00000486121.6:c.1044+46C= (GLA)
ENST00000649178.1:c.1122+46C= (GLA) ENSP00000498186.1:n.1122+46C=
ENST00000674127.1:c.1099+46C= (GLA) ENSP00000501044.1:n.1099+46C=
ENST00000674142.1:n.1303+46C= (GLA)
ENST00000674634.2:c.1045C= (GLA) ENSP00000502629.2:p.Gln349=
ENST00000675592.1:c.802-225C= (GLA) ENSP00000502239.1:n.802-225C=
ENST00000675799.1:c.*524+46C= (GLA) ENSP00000502661.1:n.*524+46C=
ENST00000675968.1:n.3870+46C= (GLA)
ENST00000676156.1:c.963+46C= (GLA) ENSP00000501730.1:n.963+46C=
ENST00000676372.1:c.1065+46C= (GLA) ENSP00000502805.1:n.1065+46C=
ENST00000218516.3:c.999+46C= (GLA) ENSP00000218516.3:n.999+46C=
ENST00000409170.3:c.300+2867G= (RPL36A-HNRNPH2) ENSP00000386655.4:n.300+2867G=
ENST00000409338.5:c.177+6502G= (RPL36A-HNRNPH2) ENSP00000386974.2:n.177+6502G=
ENST00000466414.1:n.325+46C= (GLA)
ENST00000493905.6:c.*387+46C= (GLA) ENSP00000476935.1:n.*387+46C=
NM_000169.2:c.999+46C= , LRG_672t1:c.999+46C= (GLA) NP_000160.1:n.999+46C=
NM_001199973.1:c.408+2867G= (RPL36A-HNRNPH2) NP_001186902.1:n.408+2867G=
NM_001199974.1:c.285+6502G= (RPL36A-HNRNPH2) NP_001186903.1:n.285+6502G=
XR_938397.1:n.1084+46C= (GLA)
XR_938397.2:n.1105+46C= (GLA)
NM_001199973.2:c.300+2867G= (RPL36A-HNRNPH2) NP_001186902.2:n.300+2867G=
NM_001199974.2:c.177+6502G= (RPL36A-HNRNPH2) NP_001186903.2:n.177+6502G=
NM_000169.3:c.999+46C= (GLA) MANE Select NP_000160.1:n.999+46C=
NR_164783.1:n.1078+46C= (GLA)