Canonical Allele Identifier: CA2694298592

Gene: GLA RPL36A-HNRNPH2

Linked Data

• gnomAD v4: X-101400650-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.101400650G>C , CM000685.2:g.101400650G>C	GRCh38
NC_000023.10:g.100655638G>C , CM000685.1:g.100655638G>C	GRCh37
NC_000023.9:g.100542294G>C	NCBI36
NG_007119.1:g.12314C>G , LRG_672:g.12314C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000486121.7:c.*85+16C>G (GLA)	ENSP00000501124.2:n.*85+16C>G
ENST00000674127.2:c.*85+16C>G (GLA)	ENSP00000501044.2:n.*85+16C>G
ENST00000710365.1:c.714+16C>G (GLA)	ENSP00000518234.1:n.714+16C>G
ENST00000218516.4:c.639+16C>G (GLA) MANE Select	ENSP00000218516.4:n.639+16C>G
ENST00000466414.2:n.558+16C>G (GLA)
ENST00000468823.2:n.1574+16C>G (GLA)
ENST00000479445.2:n.1036+16C>G (GLA)
ENST00000480513.6:c.547+982C>G (GLA)	ENSP00000497055.1:n.547+982C>G
ENST00000486121.6:c.684+16C>G (GLA)
ENST00000649178.1:c.762+16C>G (GLA)	ENSP00000498186.1:n.762+16C>G
ENST00000674127.1:c.682+16C>G (GLA)	ENSP00000501044.1:n.682+16C>G
ENST00000674142.1:n.726+16C>G (GLA)
ENST00000674634.2:c.639+16C>G (GLA)	ENSP00000502629.2:n.639+16C>G
ENST00000675592.1:c.639+16C>G (GLA)	ENSP00000502239.1:n.639+16C>G
ENST00000675799.1:c.547+982C>G (GLA)	ENSP00000502661.1:n.547+982C>G
ENST00000675968.1:n.1590C>G (GLA)
ENST00000676156.1:c.603+16C>G (GLA)	ENSP00000501730.1:n.603+16C>G
ENST00000676372.1:c.639+16C>G (GLA)	ENSP00000502805.1:n.639+16C>G
ENST00000218516.3:c.639+16C>G (GLA)	ENSP00000218516.3:n.639+16C>G
ENST00000409170.3:c.300+5193G>C (RPL36A-HNRNPH2)	ENSP00000386655.4:n.300+5193G>C
ENST00000409338.5:c.177+8828G>C (RPL36A-HNRNPH2)	ENSP00000386974.2:n.177+8828G>C
ENST00000468823.1:n.188+16C>G (GLA)
ENST00000480513.5:n.477+982C>G (GLA)
ENST00000486121.5:n.684+16C>G (GLA)
ENST00000493905.6:c.639+16C>G (GLA)	ENSP00000476935.1:n.639+16C>G
NM_000169.2:c.639+16C>G , LRG_672t1:c.639+16C>G (GLA)	NP_000160.1:n.639+16C>G
NM_001199973.1:c.408+5193G>C (RPL36A-HNRNPH2)	NP_001186902.1:n.408+5193G>C
NM_001199974.1:c.285+8828G>C (RPL36A-HNRNPH2)	NP_001186903.1:n.285+8828G>C
XR_938397.1:n.667+16C>G (GLA)
XR_938397.2:n.688+16C>G (GLA)
NM_001199973.2:c.300+5193G>C (RPL36A-HNRNPH2)	NP_001186902.2:n.300+5193G>C
NM_001199974.2:c.177+8828G>C (RPL36A-HNRNPH2)	NP_001186903.2:n.177+8828G>C
NM_000169.3:c.639+16C>G (GLA) MANE Select	NP_000160.1:n.639+16C>G
NR_164783.1:n.661+16C>G (GLA)