Canonical Allele Identifier: CA415258706

Gene: EMD

Linked Data

• MyVariant Identifiers: chrX:g.153609319C>G (hg19) ; chrX:g.154380959C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154380959C>G , CM000685.2:g.154380959C>G	GRCh38
NC_000023.10:g.153609319C>G , CM000685.1:g.153609319C>G	GRCh37
NC_000023.9:g.153262513C>G	NCBI36
NG_008677.1:g.11524C>G , LRG_745:g.11524C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682114.1:c.527C>G	ENSP00000507245.1:p.Ser176Cys
ENST00000682478.1:n.717C>G
ENST00000683576.1:n.717C>G
ENST00000683627.1:c.527C>G	ENSP00000507533.1:p.Ser176Cys
ENST00000684082.1:c.484C>G	ENSP00000508266.1:n.484C>G
ENST00000684633.1:n.499C>G
ENST00000684678.1:c.523C>G	ENSP00000507059.1:n.523C>G
ENST00000369842.9:c.527C>G MANE Select	ENSP00000358857.4:p.Ser176Cys
ENST00000369835.3:c.422C>G	ENSP00000358850.3:p.Ser141Cys
ENST00000369842.8:c.527C>G	ENSP00000358857.4:p.Ser176Cys
ENST00000428228.5:c.*432C>G	ENSP00000401081.1:n.*432C>G
ENST00000471965.1:n.316C>G
ENST00000486738.5:n.964C>G
ENST00000492448.1:n.510C>G
NM_000117.2:c.527C>G , LRG_745t1:c.527C>G	NP_000108.1:p.Ser176Cys
XM_024452349.1:c.533C>G	XP_024308117.1:p.Ser178Cys
NM_000117.3:c.527C>G MANE Select	NP_000108.1:p.Ser176Cys