Canonical Allele Identifier: CA519709822

Gene: EMD

Linked Data

• MyVariant Identifiers: chrX:g.153609154C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154380794C>T , CM000685.2:g.154380794C>T	GRCh38
NC_000023.10:g.153609154C>T , CM000685.1:g.153609154C>T	GRCh37
NC_000023.9:g.153262348C>T	NCBI36
NG_008677.1:g.11359C>T , LRG_745:g.11359C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000682114.1:c.441C>T	ENSP00000507245.1:p.Cys147=
ENST00000682478.1:n.631C>T
ENST00000683576.1:n.631C>T
ENST00000683627.1:c.441C>T	ENSP00000507533.1:p.Cys147=
ENST00000684082.1:c.398C>T	ENSP00000508266.1:n.398C>T
ENST00000684633.1:n.413C>T
ENST00000684678.1:c.437C>T	ENSP00000507059.1:n.437C>T
ENST00000369842.9:c.441C>T MANE Select	ENSP00000358857.4:p.Cys147=
ENST00000369835.3:c.336C>T	ENSP00000358850.3:p.Cys112=
ENST00000369842.8:c.441C>T	ENSP00000358857.4:p.Cys147=
ENST00000428228.5:c.*346C>T	ENSP00000401081.1:n.*346C>T
ENST00000468294.5:n.401C>T
ENST00000471965.1:n.230C>T
ENST00000485261.1:n.631C>T
ENST00000486738.5:n.799C>T
ENST00000492448.1:n.424C>T
NM_000117.2:c.441C>T , LRG_745t1:c.441C>T	NP_000108.1:p.Cys147=
XM_024452349.1:c.447C>T	XP_024308117.1:p.Cys149=
NM_000117.3:c.441C>T MANE Select	NP_000108.1:p.Cys147=