Canonical Allele Identifier: CA519709928

Gene: EMD

Linked Data

• MyVariant Identifiers: chrX:g.153609260C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154380900C>T , CM000685.2:g.154380900C>T	GRCh38
NC_000023.10:g.153609260C>T , CM000685.1:g.153609260C>T	GRCh37
NC_000023.9:g.153262454C>T	NCBI36
NG_008677.1:g.11465C>T , LRG_745:g.11465C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000682114.1:c.468C>T	ENSP00000507245.1:p.Gly156=
ENST00000682478.1:n.658C>T
ENST00000683576.1:n.658C>T
ENST00000683627.1:c.468C>T	ENSP00000507533.1:p.Gly156=
ENST00000684082.1:c.425C>T	ENSP00000508266.1:n.425C>T
ENST00000684633.1:n.440C>T
ENST00000684678.1:c.464C>T	ENSP00000507059.1:n.464C>T
ENST00000369842.9:c.468C>T MANE Select	ENSP00000358857.4:p.Gly156=
ENST00000369835.3:c.363C>T	ENSP00000358850.3:p.Gly121=
ENST00000369842.8:c.468C>T	ENSP00000358857.4:p.Gly156=
ENST00000428228.5:c.*373C>T	ENSP00000401081.1:n.*373C>T
ENST00000471965.1:n.257C>T
ENST00000485261.1:n.737C>T
ENST00000486738.5:n.905C>T
ENST00000492448.1:n.451C>T
NM_000117.2:c.468C>T , LRG_745t1:c.468C>T	NP_000108.1:p.Gly156=
XM_024452349.1:c.474C>T	XP_024308117.1:p.Gly158=
NM_000117.3:c.468C>T MANE Select	NP_000108.1:p.Gly156=