Canonical Allele Identifier: CA519277780

Gene: EMD

Linked Data

• gnomAD v4: X-154379508-G-A
• MyVariant Identifiers: chrX:g.153607868G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154379508G>A , CM000685.2:g.154379508G>A	GRCh38
NC_000023.10:g.153607868G>A , CM000685.1:g.153607868G>A	GRCh37
NC_000023.9:g.153261062G>A	NCBI36
NG_008677.1:g.10073G>A , LRG_745:g.10073G>A
NG_011506.1:g.139C>T
NG_011506.2:g.131C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682114.1:c.24G>A	ENSP00000507245.1:p.Ser8=
ENST00000683627.1:c.24G>A	ENSP00000507533.1:p.Ser8=
ENST00000684082.1:c.24G>A	ENSP00000508266.1:p.Ser8=
ENST00000684678.1:c.24G>A	ENSP00000507059.1:p.Ser8=
ENST00000369842.9:c.24G>A MANE Select	ENSP00000358857.4:p.Ser8=
ENST00000369835.3:c.24G>A	ENSP00000358850.3:p.Ser8=
ENST00000369842.8:c.24G>A	ENSP00000358857.4:p.Ser8=
ENST00000428228.5:c.24G>A	ENSP00000401081.1:p.Ser8=
ENST00000485261.1:n.105G>A
ENST00000486738.5:n.168G>A
ENST00000494443.5:n.81G>A
NM_000117.2:c.24G>A , LRG_745t1:c.24G>A	NP_000108.1:p.Ser8=
XM_024452349.1:c.-185G>A	XP_024308117.1:n.-185G>A
NM_000117.3:c.24G>A MANE Select	NP_000108.1:p.Ser8=