Canonical Allele Identifier: CA352605
Community Standard Title: NM_000169.3(GLA):c.1156C>T (p.Gln386Ter)
Gene: GLA HGNC NCBI
RPL36A-HNRNPH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101397943G>A , CM000685.2:g.101397943G>A GRCh38
NC_000023.10:g.100652931G>A , CM000685.1:g.100652931G>A GRCh37
NC_000023.9:g.100539587G>A NCBI36
NG_007119.1:g.15021C>T , LRG_672:g.15021C>T

Transcript Alleles

HGVS Amino-acid Change
NM_000169.3:c.1156C>T (GLA) MANE Select NP_000160.1:p.Gln386Ter
ENST00000218516.4:c.1156C>T (GLA) MANE Select ENSP00000218516.4:p.Gln386Ter
NM_000169.2:c.1156C>T , LRG_672t1:c.1156C>T (GLA) NP_000160.1:p.Gln386Ter
NM_001199973.1:c.408+2486G>A (RPL36A-HNRNPH2) NP_001186902.1:n.408+2486G>A
NM_001199973.2:c.300+2486G>A (RPL36A-HNRNPH2) NP_001186902.2:n.300+2486G>A
NM_001199974.1:c.285+6121G>A (RPL36A-HNRNPH2) NP_001186903.1:n.285+6121G>A
NM_001199974.2:c.177+6121G>A (RPL36A-HNRNPH2) NP_001186903.2:n.177+6121G>A
NR_164783.1:n.1235C>T (GLA)
ENST00000218516.3:c.1156C>T (GLA) ENSP00000218516.3:p.Gln386Ter
ENST00000409170.3:c.300+2486G>A (RPL36A-HNRNPH2) ENSP00000386655.4:n.300+2486G>A
ENST00000409338.5:c.177+6121G>A (RPL36A-HNRNPH2) ENSP00000386974.2:n.177+6121G>A
ENST00000466414.1:n.482C>T (GLA)
ENST00000466414.2:n.1292C>T (GLA)
ENST00000468823.2:n.2578C>T (GLA)
ENST00000479445.2:n.1770C>T (GLA)
ENST00000480513.6:c.*464C>T (GLA) ENSP00000497055.1:n.*464C>T
ENST00000486121.6:c.1201C>T (GLA)
ENST00000486121.7:c.*602C>T (GLA) ENSP00000501124.2:n.*602C>T
ENST00000493905.6:c.*544C>T (GLA) ENSP00000476935.1:n.*544C>T
ENST00000649178.1:c.1279C>T (GLA) ENSP00000498186.1:p.Gln427Ter
ENST00000674127.1:c.1256C>T (GLA) ENSP00000501044.1:n.1256C>T
ENST00000674127.2:c.*659C>T (GLA) ENSP00000501044.2:n.*659C>T
ENST00000674142.1:n.1421+39C>T (GLA)
ENST00000675592.1:c.958C>T (GLA) ENSP00000502239.1:p.Gln320Ter
ENST00000675799.1:c.*681C>T (GLA) ENSP00000502661.1:n.*681C>T
ENST00000675968.1:n.4027C>T (GLA)
ENST00000676156.1:c.1120C>T (GLA) ENSP00000501730.1:p.Gln374Ter
ENST00000676372.1:c.1222C>T (GLA) ENSP00000502805.1:n.1222C>T
ENST00000710365.1:c.1231C>T (GLA) ENSP00000518234.1:p.Gln411Ter
XR_938397.1:n.1241C>T (GLA)
XR_938397.2:n.1262C>T (GLA)