Canonical Allele Identifier: CA415257527

Gene: EMD

Linked Data

• MyVariant Identifiers: chrX:g.153608134C>A (hg19) ; chrX:g.154379774C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154379774C>A , CM000685.2:g.154379774C>A	GRCh38
NC_000023.10:g.153608134C>A , CM000685.1:g.153608134C>A	GRCh37
NC_000023.9:g.153261328C>A	NCBI36
NG_008677.1:g.10339C>A , LRG_745:g.10339C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682114.1:c.167C>A	ENSP00000507245.1:p.Ala56Asp
ENST00000682478.1:n.143C>A
ENST00000683576.1:n.143C>A
ENST00000683627.1:c.167C>A	ENSP00000507533.1:p.Ala56Asp
ENST00000684082.1:c.167C>A	ENSP00000508266.1:p.Ala56Asp
ENST00000684633.1:n.139C>A
ENST00000684678.1:c.163C>A	ENSP00000507059.1:p.Pro55Thr
ENST00000369842.9:c.167C>A MANE Select	ENSP00000358857.4:p.Ala56Asp
ENST00000369835.3:c.83-168C>A	ENSP00000358850.3:n.83-168C>A
ENST00000369842.8:c.167C>A	ENSP00000358857.4:p.Ala56Asp
ENST00000428228.5:c.*72C>A	ENSP00000401081.1:n.*72C>A
ENST00000468294.5:n.127C>A
ENST00000485261.1:n.164-168C>A
ENST00000486738.5:n.311C>A
ENST00000492448.1:n.150C>A
ENST00000494443.5:n.224C>A
NM_000117.2:c.167C>A , LRG_745t1:c.167C>A	NP_000108.1:p.Ala56Asp
XM_024452349.1:c.-42C>A	XP_024308117.1:n.-42C>A
NM_000117.3:c.167C>A MANE Select	NP_000108.1:p.Ala56Asp