Canonical Allele Identifier: CA519709847

Gene: EMD

Linked Data

• MyVariant Identifiers: chrX:g.153609161A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154380801A>C , CM000685.2:g.154380801A>C	GRCh38
NC_000023.10:g.153609161A>C , CM000685.1:g.153609161A>C	GRCh37
NC_000023.9:g.153262355A>C	NCBI36
NG_008677.1:g.11366A>C , LRG_745:g.11366A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682114.1:c.448A>C	ENSP00000507245.1:p.Arg150=
ENST00000682478.1:n.638A>C
ENST00000683576.1:n.638A>C
ENST00000683627.1:c.448A>C	ENSP00000507533.1:p.Arg150=
ENST00000684082.1:c.405A>C	ENSP00000508266.1:n.405A>C
ENST00000684633.1:n.420A>C
ENST00000684678.1:c.444A>C	ENSP00000507059.1:n.444A>C
ENST00000369842.9:c.448A>C MANE Select	ENSP00000358857.4:p.Arg150=
ENST00000369835.3:c.343A>C	ENSP00000358850.3:p.Arg115=
ENST00000369842.8:c.448A>C	ENSP00000358857.4:p.Arg150=
ENST00000428228.5:c.*353A>C	ENSP00000401081.1:n.*353A>C
ENST00000468294.5:n.408A>C
ENST00000471965.1:n.237A>C
ENST00000485261.1:n.638A>C
ENST00000486738.5:n.806A>C
ENST00000492448.1:n.431A>C
NM_000117.2:c.448A>C , LRG_745t1:c.448A>C	NP_000108.1:p.Arg150=
XM_024452349.1:c.454A>C	XP_024308117.1:p.Arg152=
NM_000117.3:c.448A>C MANE Select	NP_000108.1:p.Arg150=