Canonical Allele Identifier: CA413927949

Gene: GLA RPL36A-HNRNPH2

Linked Data

• MyVariant Identifiers: chrX:g.100655740T>G (hg19) ; chrX:g.101400752T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.101400752T>G , CM000685.2:g.101400752T>G	GRCh38
NC_000023.10:g.100655740T>G , CM000685.1:g.100655740T>G	GRCh37
NC_000023.9:g.100542396T>G	NCBI36
NG_007119.1:g.12212A>C , LRG_672:g.12212A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000486121.7:c.668A>C (GLA)	ENSP00000501124.2:p.Ter223Ser
ENST00000674127.2:c.668A>C (GLA)	ENSP00000501044.2:p.Ter223Ser
ENST00000710365.1:c.628A>C (GLA)	ENSP00000518234.1:p.Lys210Gln
ENST00000218516.4:c.553A>C (GLA) MANE Select	ENSP00000218516.4:p.Lys185Gln
ENST00000466414.2:n.472A>C (GLA)
ENST00000468823.2:n.1488A>C (GLA)
ENST00000479445.2:n.950A>C (GLA)
ENST00000480513.6:c.547+880A>C (GLA)	ENSP00000497055.1:n.547+880A>C
ENST00000486121.6:c.598A>C (GLA)
ENST00000649178.1:c.676A>C (GLA)	ENSP00000498186.1:p.Lys226Gln
ENST00000674127.1:c.596A>C (GLA)	ENSP00000501044.1:p.Ter199Ser
ENST00000674142.1:n.640A>C (GLA)
ENST00000674634.2:c.553A>C (GLA)	ENSP00000502629.2:p.Lys185Gln
ENST00000675592.1:c.553A>C (GLA)	ENSP00000502239.1:p.Lys185Gln
ENST00000675799.1:c.547+880A>C (GLA)	ENSP00000502661.1:n.547+880A>C
ENST00000675968.1:n.1488A>C (GLA)
ENST00000676156.1:c.517A>C (GLA)	ENSP00000501730.1:p.Lys173Gln
ENST00000676372.1:c.553A>C (GLA)	ENSP00000502805.1:p.Lys185Gln
ENST00000218516.3:c.553A>C (GLA)	ENSP00000218516.3:p.Lys185Gln
ENST00000409170.3:c.300+5295T>G (RPL36A-HNRNPH2)	ENSP00000386655.4:n.300+5295T>G
ENST00000409338.5:c.177+8930T>G (RPL36A-HNRNPH2)	ENSP00000386974.2:n.177+8930T>G
ENST00000468823.1:n.102A>C (GLA)
ENST00000480513.5:n.477+880A>C (GLA)
ENST00000486121.5:n.598A>C (GLA)
ENST00000493905.6:c.553A>C (GLA)	ENSP00000476935.1:p.Lys185Gln
NM_000169.2:c.553A>C , LRG_672t1:c.553A>C (GLA)	NP_000160.1:p.Lys185Gln
NM_001199973.1:c.408+5295T>G (RPL36A-HNRNPH2)	NP_001186902.1:n.408+5295T>G
NM_001199974.1:c.285+8930T>G (RPL36A-HNRNPH2)	NP_001186903.1:n.285+8930T>G
XR_938397.1:n.581A>C (GLA)
XR_938397.2:n.602A>C (GLA)
NM_001199973.2:c.300+5295T>G (RPL36A-HNRNPH2)	NP_001186902.2:n.300+5295T>G
NM_001199974.2:c.177+8930T>G (RPL36A-HNRNPH2)	NP_001186903.2:n.177+8930T>G
NM_000169.3:c.553A>C (GLA) MANE Select	NP_000160.1:p.Lys185Gln
NR_164783.1:n.575A>C (GLA)