Canonical Allele Identifier: CA413925122

Gene: GLA RPL36A-HNRNPH2

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.101398940A>C , CM000685.2:g.101398940A>C	GRCh38
NC_000023.10:g.100653928A>C , CM000685.1:g.100653928A>C	GRCh37
NC_000023.9:g.100540584A>C	NCBI36
NG_007119.1:g.14024T>G , LRG_672:g.14024T>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000169.3:c.646T>G (GLA) MANE Select	NP_000160.1:p.Tyr216Asp
ENST00000218516.4:c.646T>G (GLA) MANE Select	ENSP00000218516.4:p.Tyr216Asp
NM_000169.2:c.646T>G , LRG_672t1:c.646T>G (GLA)	NP_000160.1:p.Tyr216Asp
NM_001199973.1:c.408+3483A>C (RPL36A-HNRNPH2)	NP_001186902.1:n.408+3483A>C
NM_001199973.2:c.300+3483A>C (RPL36A-HNRNPH2)	NP_001186902.2:n.300+3483A>C
NM_001199974.1:c.285+7118A>C (RPL36A-HNRNPH2)	NP_001186903.1:n.285+7118A>C
NM_001199974.2:c.177+7118A>C (RPL36A-HNRNPH2)	NP_001186903.2:n.177+7118A>C
NR_164783.1:n.725T>G (GLA)
ENST00000218516.3:c.646T>G (GLA)	ENSP00000218516.3:p.Tyr216Asp
ENST00000409170.3:c.300+3483A>C (RPL36A-HNRNPH2)	ENSP00000386655.4:n.300+3483A>C
ENST00000409338.5:c.177+7118A>C (RPL36A-HNRNPH2)	ENSP00000386974.2:n.177+7118A>C
ENST00000466414.2:n.565T>G (GLA)
ENST00000468823.1:n.195T>G (GLA)
ENST00000468823.2:n.1581T>G (GLA)
ENST00000479445.2:n.1043T>G (GLA)
ENST00000480513.5:n.484T>G (GLA)
ENST00000480513.6:c.554T>G (GLA)	ENSP00000497055.1:p.Leu185Ter
ENST00000486121.5:n.691T>G (GLA)
ENST00000486121.6:c.691T>G (GLA)
ENST00000486121.7:c.*92T>G (GLA)	ENSP00000501124.2:n.*92T>G
ENST00000493905.6:c.*34T>G (GLA)	ENSP00000476935.1:n.*34T>G
ENST00000649178.1:c.769T>G (GLA)	ENSP00000498186.1:p.Tyr257Asp
ENST00000674127.1:c.746T>G (GLA)	ENSP00000501044.1:n.746T>G
ENST00000674127.2:c.*149T>G (GLA)	ENSP00000501044.2:n.*149T>G
ENST00000674142.1:n.733T>G (GLA)
ENST00000674634.2:c.646T>G (GLA)	ENSP00000502629.2:p.Tyr216Asp
ENST00000675592.1:c.646T>G (GLA)	ENSP00000502239.1:p.Tyr216Asp
ENST00000675799.1:c.554T>G (GLA)	ENSP00000502661.1:p.Leu185Ter
ENST00000675968.1:n.3300T>G (GLA)
ENST00000676156.1:c.610T>G (GLA)	ENSP00000501730.1:p.Tyr204Asp
ENST00000676372.1:c.646T>G (GLA)	ENSP00000502805.1:p.Tyr216Asp
ENST00000710365.1:c.721T>G (GLA)	ENSP00000518234.1:p.Tyr241Asp
XR_938397.1:n.731T>G (GLA)
XR_938397.2:n.752T>G (GLA)