Canonical Allele Identifier: CA2579664581
Gene: GLA HGNC NCBI
RPL36A-HNRNPH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101398159G>T , CM000685.2:g.101398159G>T GRCh38
NC_000023.10:g.100653147G>T , CM000685.1:g.100653147G>T GRCh37
NC_000023.9:g.100539803G>T NCBI36
NG_007119.1:g.14805C>A , LRG_672:g.14805C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000486121.7:c.*446-60C>A (GLA) ENSP00000501124.2:n.*446-60C>A
ENST00000674127.2:c.*503-60C>A (GLA) ENSP00000501044.2:n.*503-60C>A
ENST00000710365.1:c.1075-60C>A (GLA) ENSP00000518234.1:n.1075-60C>A
ENST00000218516.4:c.1000-60C>A (GLA) MANE Select ENSP00000218516.4:n.1000-60C>A
ENST00000466414.2:n.1136-60C>A (GLA)
ENST00000468823.2:n.2362C>A (GLA)
ENST00000479445.2:n.1614-60C>A (GLA)
ENST00000480513.6:c.*308-60C>A (GLA) ENSP00000497055.1:n.*308-60C>A
ENST00000486121.6:c.1045-60C>A (GLA)
ENST00000649178.1:c.1123-60C>A (GLA) ENSP00000498186.1:n.1123-60C>A
ENST00000674127.1:c.1100-60C>A (GLA) ENSP00000501044.1:n.1100-60C>A
ENST00000674142.1:n.1304-60C>A (GLA)
ENST00000675592.1:c.802-60C>A (GLA) ENSP00000502239.1:n.802-60C>A
ENST00000675799.1:c.*525-60C>A (GLA) ENSP00000502661.1:n.*525-60C>A
ENST00000675968.1:n.3871-60C>A (GLA)
ENST00000676156.1:c.964-60C>A (GLA) ENSP00000501730.1:n.964-60C>A
ENST00000676372.1:c.1066-60C>A (GLA) ENSP00000502805.1:n.1066-60C>A
ENST00000218516.3:c.1000-60C>A (GLA) ENSP00000218516.3:n.1000-60C>A
ENST00000409170.3:c.300+2702G>T (RPL36A-HNRNPH2) ENSP00000386655.4:n.300+2702G>T
ENST00000409338.5:c.177+6337G>T (RPL36A-HNRNPH2) ENSP00000386974.2:n.177+6337G>T
ENST00000466414.1:n.326-60C>A (GLA)
ENST00000493905.6:c.*388-60C>A (GLA) ENSP00000476935.1:n.*388-60C>A
NM_000169.2:c.1000-60C>A , LRG_672t1:c.1000-60C>A (GLA) NP_000160.1:n.1000-60C>A
NM_001199973.1:c.408+2702G>T (RPL36A-HNRNPH2) NP_001186902.1:n.408+2702G>T
NM_001199974.1:c.285+6337G>T (RPL36A-HNRNPH2) NP_001186903.1:n.285+6337G>T
XR_938397.1:n.1085-60C>A (GLA)
XR_938397.2:n.1106-60C>A (GLA)
NM_001199973.2:c.300+2702G>T (RPL36A-HNRNPH2) NP_001186902.2:n.300+2702G>T
NM_001199974.2:c.177+6337G>T (RPL36A-HNRNPH2) NP_001186903.2:n.177+6337G>T
NM_000169.3:c.1000-60C>A (GLA) MANE Select NP_000160.1:n.1000-60C>A
NR_164783.1:n.1079-60C>A (GLA)