Canonical Allele Identifier: CA2448299918

Gene: GLA RPL36A-HNRNPH2

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.101403994G= , CM000685.2:g.101403994G=	GRCh38
NC_000023.10:g.100658982G= , CM000685.1:g.100658982G=	GRCh37
NC_000023.9:g.100545638G=	NCBI36
NG_007119.1:g.8970C= , LRG_672:g.8970C=
NG_016327.1:g.792G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000486121.7:c.195-9C= (GLA)	ENSP00000501124.2:n.195-9C=
ENST00000674127.2:c.195-9C= (GLA)	ENSP00000501044.2:n.195-9C=
ENST00000710365.1:c.270-9C= (GLA)	ENSP00000518234.1:n.270-9C=
ENST00000218516.4:c.195-9C= (GLA) MANE Select	ENSP00000218516.4:n.195-9C=
ENST00000466414.2:n.114-9C= (GLA)
ENST00000468823.2:n.256-9C= (GLA)
ENST00000479445.2:n.193-9C= (GLA)
ENST00000480513.6:c.195-9C= (GLA)	ENSP00000497055.1:n.195-9C=
ENST00000486121.6:c.125-9C= (GLA)
ENST00000649178.1:c.318-9C= (GLA)	ENSP00000498186.1:n.318-9C=
ENST00000674127.1:c.123-9C= (GLA)	ENSP00000501044.1:n.123-9C=
ENST00000674142.1:n.282-9C= (GLA)
ENST00000674634.2:c.195-9C= (GLA)	ENSP00000502629.2:n.195-9C=
ENST00000675592.1:c.195-9C= (GLA)	ENSP00000502239.1:n.195-9C=
ENST00000675799.1:c.195-9C= (GLA)	ENSP00000502661.1:n.195-9C=
ENST00000675968.1:n.256-9C= (GLA)
ENST00000676156.1:c.195-9C= (GLA)	ENSP00000501730.1:n.195-9C=
ENST00000676372.1:c.195-9C= (GLA)	ENSP00000502805.1:n.195-9C=
ENST00000218516.3:c.195-9C= (GLA)	ENSP00000218516.3:n.195-9C=
ENST00000409170.3:c.301-7942G= (RPL36A-HNRNPH2)	ENSP00000386655.4:n.301-7942G=
ENST00000409338.5:c.178-7942G= (RPL36A-HNRNPH2)	ENSP00000386974.2:n.178-7942G=
ENST00000479445.1:n.179-9C= (GLA)
ENST00000480513.5:n.125-9C= (GLA)
ENST00000486121.5:n.125-9C= (GLA)
ENST00000493905.6:c.195-9C= (GLA)	ENSP00000476935.1:n.195-9C=
NM_000169.2:c.195-9C= , LRG_672t1:c.195-9C= (GLA)	NP_000160.1:n.195-9C=
NM_001199973.1:c.409-7942G= (RPL36A-HNRNPH2)	NP_001186902.1:n.409-7942G=
NM_001199974.1:c.286-7942G= (RPL36A-HNRNPH2)	NP_001186903.1:n.286-7942G=
XR_938397.1:n.223-9C= (GLA)
XR_938397.2:n.244-9C= (GLA)
NM_001199973.2:c.301-7942G= (RPL36A-HNRNPH2)	NP_001186902.2:n.301-7942G=
NM_001199974.2:c.178-7942G= (RPL36A-HNRNPH2)	NP_001186903.2:n.178-7942G=
NM_000169.3:c.195-9C= (GLA) MANE Select	NP_000160.1:n.195-9C=
NR_164783.1:n.217-9C= (GLA)