Canonical Allele Identifier: CA2448299170

Gene: GLA RPL36A-HNRNPH2

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.101401735A= , CM000685.2:g.101401735A=	GRCh38
NC_000023.10:g.100656723A= , CM000685.1:g.100656723A=	GRCh37
NC_000023.9:g.100543379A=	NCBI36
NG_007119.1:g.11229T= , LRG_672:g.11229T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000486121.7:c.444T= (GLA)	ENSP00000501124.2:p.Ser148=
ENST00000674127.2:c.444T= (GLA)	ENSP00000501044.2:p.Ser148=
ENST00000710365.1:c.519T= (GLA)	ENSP00000518234.1:p.Ser173=
ENST00000218516.4:c.444T= (GLA) MANE Select	ENSP00000218516.4:p.Ser148=
ENST00000466414.2:n.363T= (GLA)
ENST00000468823.2:n.505T= (GLA)
ENST00000479445.2:n.442T= (GLA)
ENST00000480513.6:c.444T= (GLA)	ENSP00000497055.1:p.Ser148=
ENST00000486121.6:c.374T= (GLA)
ENST00000649178.1:c.567T= (GLA)	ENSP00000498186.1:p.Ser189=
ENST00000674127.1:c.372T= (GLA)	ENSP00000501044.1:p.Ser124=
ENST00000674142.1:n.531T= (GLA)
ENST00000674634.2:c.444T= (GLA)	ENSP00000502629.2:p.Ser148=
ENST00000675592.1:c.444T= (GLA)	ENSP00000502239.1:p.Ser148=
ENST00000675799.1:c.444T= (GLA)	ENSP00000502661.1:p.Ser148=
ENST00000675968.1:n.505T= (GLA)
ENST00000676156.1:c.444T= (GLA)	ENSP00000501730.1:p.Ser148=
ENST00000676372.1:c.444T= (GLA)	ENSP00000502805.1:p.Ser148=
ENST00000218516.3:c.444T= (GLA)	ENSP00000218516.3:p.Ser148=
ENST00000409170.3:c.300+6278A= (RPL36A-HNRNPH2)	ENSP00000386655.4:n.300+6278A=
ENST00000409338.5:c.177+9913A= (RPL36A-HNRNPH2)	ENSP00000386974.2:n.177+9913A=
ENST00000479445.1:n.428T= (GLA)
ENST00000480513.5:n.374T= (GLA)
ENST00000486121.5:n.374T= (GLA)
ENST00000493905.6:c.444T= (GLA)	ENSP00000476935.1:p.Ser148=
NM_000169.2:c.444T= , LRG_672t1:c.444T= (GLA)	NP_000160.1:p.Ser148=
NM_001199973.1:c.408+6278A= (RPL36A-HNRNPH2)	NP_001186902.1:n.408+6278A=
NM_001199974.1:c.285+9913A= (RPL36A-HNRNPH2)	NP_001186903.1:n.285+9913A=
XR_938397.1:n.472T= (GLA)
XR_938397.2:n.493T= (GLA)
NM_001199973.2:c.300+6278A= (RPL36A-HNRNPH2)	NP_001186902.2:n.300+6278A=
NM_001199974.2:c.177+9913A= (RPL36A-HNRNPH2)	NP_001186903.2:n.177+9913A=
NM_000169.3:c.444T= (GLA) MANE Select	NP_000160.1:p.Ser148=
NR_164783.1:n.466T= (GLA)