Canonical Allele Identifier: CA2694298348

Gene: GLA RPL36A-HNRNPH2

Linked Data

• gnomAD v4: X-101398707-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.101398707A>G , CM000685.2:g.101398707A>G	GRCh38
NC_000023.10:g.100653695A>G , CM000685.1:g.100653695A>G	GRCh37
NC_000023.9:g.100540351A>G	NCBI36
NG_007119.1:g.14257T>C , LRG_672:g.14257T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000486121.7:c.*247+78T>C (GLA)	ENSP00000501124.2:n.*247+78T>C
ENST00000674127.2:c.*304+78T>C (GLA)	ENSP00000501044.2:n.*304+78T>C
ENST00000710365.1:c.876+78T>C (GLA)	ENSP00000518234.1:n.876+78T>C
ENST00000218516.4:c.801+78T>C (GLA) MANE Select	ENSP00000218516.4:n.801+78T>C
ENST00000466414.2:n.798T>C (GLA)
ENST00000468823.2:n.1814T>C (GLA)
ENST00000479445.2:n.1276T>C (GLA)
ENST00000480513.6:c.*109+78T>C (GLA)	ENSP00000497055.1:n.*109+78T>C
ENST00000486121.6:c.846+78T>C (GLA)
ENST00000649178.1:c.924+78T>C (GLA)	ENSP00000498186.1:n.924+78T>C
ENST00000674127.1:c.901+78T>C (GLA)	ENSP00000501044.1:n.901+78T>C
ENST00000674142.1:n.966T>C (GLA)
ENST00000674634.2:c.801+78T>C (GLA)	ENSP00000502629.2:n.801+78T>C
ENST00000675592.1:c.801+78T>C (GLA)	ENSP00000502239.1:n.801+78T>C
ENST00000675799.1:c.*187T>C (GLA)	ENSP00000502661.1:n.*187T>C
ENST00000675968.1:n.3533T>C (GLA)
ENST00000676156.1:c.765+78T>C (GLA)	ENSP00000501730.1:n.765+78T>C
ENST00000676372.1:c.867+12T>C (GLA)	ENSP00000502805.1:n.867+12T>C
ENST00000218516.3:c.801+78T>C (GLA)	ENSP00000218516.3:n.801+78T>C
ENST00000409170.3:c.300+3250A>G (RPL36A-HNRNPH2)	ENSP00000386655.4:n.300+3250A>G
ENST00000409338.5:c.177+6885A>G (RPL36A-HNRNPH2)	ENSP00000386974.2:n.177+6885A>G
ENST00000468823.1:n.428T>C (GLA)
ENST00000493905.6:c.*189+78T>C (GLA)	ENSP00000476935.1:n.*189+78T>C
NM_000169.2:c.801+78T>C , LRG_672t1:c.801+78T>C (GLA)	NP_000160.1:n.801+78T>C
NM_001199973.1:c.408+3250A>G (RPL36A-HNRNPH2)	NP_001186902.1:n.408+3250A>G
NM_001199974.1:c.285+6885A>G (RPL36A-HNRNPH2)	NP_001186903.1:n.285+6885A>G
XR_938397.1:n.886+78T>C (GLA)
XR_938397.2:n.907+78T>C (GLA)
NM_001199973.2:c.300+3250A>G (RPL36A-HNRNPH2)	NP_001186902.2:n.300+3250A>G
NM_001199974.2:c.177+6885A>G (RPL36A-HNRNPH2)	NP_001186903.2:n.177+6885A>G
NM_000169.3:c.801+78T>C (GLA) MANE Select	NP_000160.1:n.801+78T>C
NR_164783.1:n.880+78T>C (GLA)