Canonical Allele Identifier: CA2694298207

Gene: GLA RPL36A-HNRNPH2

Linked Data

• gnomAD v4: X-101398146-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.101398146G>T , CM000685.2:g.101398146G>T	GRCh38
NC_000023.10:g.100653134G>T , CM000685.1:g.100653134G>T	GRCh37
NC_000023.9:g.100539790G>T	NCBI36
NG_007119.1:g.14818C>A , LRG_672:g.14818C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000486121.7:c.*446-47C>A (GLA)	ENSP00000501124.2:n.*446-47C>A
ENST00000674127.2:c.*503-47C>A (GLA)	ENSP00000501044.2:n.*503-47C>A
ENST00000710365.1:c.1075-47C>A (GLA)	ENSP00000518234.1:n.1075-47C>A
ENST00000218516.4:c.1000-47C>A (GLA) MANE Select	ENSP00000218516.4:n.1000-47C>A
ENST00000466414.2:n.1136-47C>A (GLA)
ENST00000468823.2:n.2375C>A (GLA)
ENST00000479445.2:n.1614-47C>A (GLA)
ENST00000480513.6:c.*308-47C>A (GLA)	ENSP00000497055.1:n.*308-47C>A
ENST00000486121.6:c.1045-47C>A (GLA)
ENST00000649178.1:c.1123-47C>A (GLA)	ENSP00000498186.1:n.1123-47C>A
ENST00000674127.1:c.1100-47C>A (GLA)	ENSP00000501044.1:n.1100-47C>A
ENST00000674142.1:n.1304-47C>A (GLA)
ENST00000675592.1:c.802-47C>A (GLA)	ENSP00000502239.1:n.802-47C>A
ENST00000675799.1:c.*525-47C>A (GLA)	ENSP00000502661.1:n.*525-47C>A
ENST00000675968.1:n.3871-47C>A (GLA)
ENST00000676156.1:c.964-47C>A (GLA)	ENSP00000501730.1:n.964-47C>A
ENST00000676372.1:c.1066-47C>A (GLA)	ENSP00000502805.1:n.1066-47C>A
ENST00000218516.3:c.1000-47C>A (GLA)	ENSP00000218516.3:n.1000-47C>A
ENST00000409170.3:c.300+2689G>T (RPL36A-HNRNPH2)	ENSP00000386655.4:n.300+2689G>T
ENST00000409338.5:c.177+6324G>T (RPL36A-HNRNPH2)	ENSP00000386974.2:n.177+6324G>T
ENST00000466414.1:n.326-47C>A (GLA)
ENST00000493905.6:c.*388-47C>A (GLA)	ENSP00000476935.1:n.*388-47C>A
NM_000169.2:c.1000-47C>A , LRG_672t1:c.1000-47C>A (GLA)	NP_000160.1:n.1000-47C>A
NM_001199973.1:c.408+2689G>T (RPL36A-HNRNPH2)	NP_001186902.1:n.408+2689G>T
NM_001199974.1:c.285+6324G>T (RPL36A-HNRNPH2)	NP_001186903.1:n.285+6324G>T
XR_938397.1:n.1085-47C>A (GLA)
XR_938397.2:n.1106-47C>A (GLA)
NM_001199973.2:c.300+2689G>T (RPL36A-HNRNPH2)	NP_001186902.2:n.300+2689G>T
NM_001199974.2:c.177+6324G>T (RPL36A-HNRNPH2)	NP_001186903.2:n.177+6324G>T
NM_000169.3:c.1000-47C>A (GLA) MANE Select	NP_000160.1:n.1000-47C>A
NR_164783.1:n.1079-47C>A (GLA)