Canonical Allele Identifier: CA519277894
Gene: EMD HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.153608105G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154379745G>A , CM000685.2:g.154379745G>A GRCh38
NC_000023.10:g.153608105G>A , CM000685.1:g.153608105G>A GRCh37
NC_000023.9:g.153261299G>A NCBI36
NG_008677.1:g.10310G>A , LRG_745:g.10310G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000682114.1:c.138G>A ENSP00000507245.1:p.Arg46=
ENST00000682478.1:n.114G>A
ENST00000683576.1:n.114G>A
ENST00000683627.1:c.138G>A ENSP00000507533.1:p.Arg46=
ENST00000684082.1:c.138G>A ENSP00000508266.1:p.Arg46=
ENST00000684633.1:n.110G>A
ENST00000684678.1:c.134G>A ENSP00000507059.1:p.Gly45Asp
ENST00000369842.9:c.138G>A MANE Select ENSP00000358857.4:p.Arg46=
ENST00000369835.3:c.82+179G>A ENSP00000358850.3:n.82+179G>A
ENST00000369842.8:c.138G>A ENSP00000358857.4:p.Arg46=
ENST00000428228.5:c.*43G>A ENSP00000401081.1:n.*43G>A
ENST00000468294.5:n.98G>A
ENST00000485261.1:n.163+179G>A
ENST00000486738.5:n.282G>A
ENST00000492448.1:n.121G>A
ENST00000494443.5:n.195G>A
NM_000117.2:c.138G>A , LRG_745t1:c.138G>A NP_000108.1:p.Arg46=
XM_024452349.1:c.-71G>A XP_024308117.1:n.-71G>A
NM_000117.3:c.138G>A MANE Select NP_000108.1:p.Arg46=