Canonical Allele Identifier: CA413921359

Gene: GLA RPL36A-HNRNPH2

Linked Data

• MyVariant Identifiers: chrX:g.100653379C>G (hg19) ; chrX:g.101398391C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.101398391C>G , CM000685.2:g.101398391C>G	GRCh38
NC_000023.10:g.100653379C>G , CM000685.1:g.100653379C>G	GRCh37
NC_000023.9:g.100540035C>G	NCBI36
NG_007119.1:g.14573G>C , LRG_672:g.14573G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000486121.7:c.*424G>C (GLA)	ENSP00000501124.2:n.*424G>C
ENST00000674127.2:c.*481G>C (GLA)	ENSP00000501044.2:n.*481G>C
ENST00000710365.1:c.1053G>C (GLA)	ENSP00000518234.1:p.Lys351Asn
ENST00000218516.4:c.978G>C (GLA) MANE Select	ENSP00000218516.4:p.Lys326Asn
ENST00000466414.2:n.1114G>C (GLA)
ENST00000468823.2:n.2130G>C (GLA)
ENST00000479445.2:n.1592G>C (GLA)
ENST00000480513.6:c.*286G>C (GLA)	ENSP00000497055.1:n.*286G>C
ENST00000486121.6:c.1023G>C (GLA)
ENST00000649178.1:c.1101G>C (GLA)	ENSP00000498186.1:p.Lys367Asn
ENST00000674127.1:c.1078G>C (GLA)	ENSP00000501044.1:n.1078G>C
ENST00000674142.1:n.1282G>C (GLA)
ENST00000674634.2:c.978G>C (GLA)	ENSP00000502629.2:p.Lys326Asn
ENST00000675592.1:c.802-292G>C (GLA)	ENSP00000502239.1:n.802-292G>C
ENST00000675799.1:c.*503G>C (GLA)	ENSP00000502661.1:n.*503G>C
ENST00000675968.1:n.3849G>C (GLA)
ENST00000676156.1:c.942G>C (GLA)	ENSP00000501730.1:p.Lys314Asn
ENST00000676372.1:c.1044G>C (GLA)	ENSP00000502805.1:n.1044G>C
ENST00000218516.3:c.978G>C (GLA)	ENSP00000218516.3:p.Lys326Asn
ENST00000409170.3:c.300+2934C>G (RPL36A-HNRNPH2)	ENSP00000386655.4:n.300+2934C>G
ENST00000409338.5:c.177+6569C>G (RPL36A-HNRNPH2)	ENSP00000386974.2:n.177+6569C>G
ENST00000466414.1:n.304G>C (GLA)
ENST00000493905.6:c.*366G>C (GLA)	ENSP00000476935.1:n.*366G>C
NM_000169.2:c.978G>C , LRG_672t1:c.978G>C (GLA)	NP_000160.1:p.Lys326Asn
NM_001199973.1:c.408+2934C>G (RPL36A-HNRNPH2)	NP_001186902.1:n.408+2934C>G
NM_001199974.1:c.285+6569C>G (RPL36A-HNRNPH2)	NP_001186903.1:n.285+6569C>G
XR_938397.1:n.1063G>C (GLA)
XR_938397.2:n.1084G>C (GLA)
NM_001199973.2:c.300+2934C>G (RPL36A-HNRNPH2)	NP_001186902.2:n.300+2934C>G
NM_001199974.2:c.177+6569C>G (RPL36A-HNRNPH2)	NP_001186903.2:n.177+6569C>G
NM_000169.3:c.978G>C (GLA) MANE Select	NP_000160.1:p.Lys326Asn
NR_164783.1:n.1057G>C (GLA)