Canonical Allele Identifier: CA413921219
Gene: GLA HGNC NCBI
RPL36A-HNRNPH2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101398084C>A , CM000685.2:g.101398084C>A GRCh38
NC_000023.10:g.100653072C>A , CM000685.1:g.100653072C>A GRCh37
NC_000023.9:g.100539728C>A NCBI36
NG_007119.1:g.14880G>T , LRG_672:g.14880G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000486121.7:c.*461G>T (GLA) ENSP00000501124.2:n.*461G>T
ENST00000674127.2:c.*518G>T (GLA) ENSP00000501044.2:n.*518G>T
ENST00000710365.1:c.1090G>T (GLA) ENSP00000518234.1:p.Val364Leu
ENST00000218516.4:c.1015G>T (GLA) MANE Select ENSP00000218516.4:p.Val339Leu
ENST00000466414.2:n.1151G>T (GLA)
ENST00000468823.2:n.2437G>T (GLA)
ENST00000479445.2:n.1629G>T (GLA)
ENST00000480513.6:c.*323G>T (GLA) ENSP00000497055.1:n.*323G>T
ENST00000486121.6:c.1060G>T (GLA)
ENST00000649178.1:c.1138G>T (GLA) ENSP00000498186.1:p.Val380Leu
ENST00000674127.1:c.1115G>T (GLA) ENSP00000501044.1:n.1115G>T
ENST00000674142.1:n.1319G>T (GLA)
ENST00000675592.1:c.817G>T (GLA) ENSP00000502239.1:p.Val273Leu
ENST00000675799.1:c.*540G>T (GLA) ENSP00000502661.1:n.*540G>T
ENST00000675968.1:n.3886G>T (GLA)
ENST00000676156.1:c.979G>T (GLA) ENSP00000501730.1:p.Val327Leu
ENST00000676372.1:c.1081G>T (GLA) ENSP00000502805.1:n.1081G>T
ENST00000218516.3:c.1015G>T (GLA) ENSP00000218516.3:p.Val339Leu
ENST00000409170.3:c.300+2627C>A (RPL36A-HNRNPH2) ENSP00000386655.4:n.300+2627C>A
ENST00000409338.5:c.177+6262C>A (RPL36A-HNRNPH2) ENSP00000386974.2:n.177+6262C>A
ENST00000466414.1:n.341G>T (GLA)
ENST00000493905.6:c.*403G>T (GLA) ENSP00000476935.1:n.*403G>T
NM_000169.2:c.1015G>T , LRG_672t1:c.1015G>T (GLA) NP_000160.1:p.Val339Leu
NM_001199973.1:c.408+2627C>A (RPL36A-HNRNPH2) NP_001186902.1:n.408+2627C>A
NM_001199974.1:c.285+6262C>A (RPL36A-HNRNPH2) NP_001186903.1:n.285+6262C>A
XR_938397.1:n.1100G>T (GLA)
XR_938397.2:n.1121G>T (GLA)
NM_001199973.2:c.300+2627C>A (RPL36A-HNRNPH2) NP_001186902.2:n.300+2627C>A
NM_001199974.2:c.177+6262C>A (RPL36A-HNRNPH2) NP_001186903.2:n.177+6262C>A
NM_000169.3:c.1015G>T (GLA) MANE Select NP_000160.1:p.Val339Leu
NR_164783.1:n.1094G>T (GLA)