Canonical Allele Identifier: CA519277835

Gene: EMD

Linked Data

• MyVariant Identifiers: chrX:g.153607925A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154379565A>T , CM000685.2:g.154379565A>T	GRCh38
NC_000023.10:g.153607925A>T , CM000685.1:g.153607925A>T	GRCh37
NC_000023.9:g.153261119A>T	NCBI36
NG_008677.1:g.10130A>T , LRG_745:g.10130A>T
NG_011506.1:g.82T>A
NG_011506.2:g.74T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000682114.1:c.81A>T	ENSP00000507245.1:p.Val27=
ENST00000682478.1:n.57A>T
ENST00000683576.1:n.57A>T
ENST00000683627.1:c.81A>T	ENSP00000507533.1:p.Val27=
ENST00000684082.1:c.81A>T	ENSP00000508266.1:p.Val27=
ENST00000684633.1:n.54+3A>T
ENST00000684678.1:c.78+3A>T	ENSP00000507059.1:n.78+3A>T
ENST00000369842.9:c.81A>T MANE Select	ENSP00000358857.4:p.Val27=
ENST00000369835.3:c.81A>T	ENSP00000358850.3:p.Val27=
ENST00000369842.8:c.81A>T	ENSP00000358857.4:p.Val27=
ENST00000428228.5:c.53+28A>T	ENSP00000401081.1:n.53+28A>T
ENST00000468294.5:n.41A>T
ENST00000485261.1:n.162A>T
ENST00000486738.5:n.225A>T
ENST00000494443.5:n.138A>T
NM_000117.2:c.81A>T , LRG_745t1:c.81A>T	NP_000108.1:p.Val27=
XM_024452349.1:c.-128A>T	XP_024308117.1:n.-128A>T
NM_000117.3:c.81A>T MANE Select	NP_000108.1:p.Val27=