Canonical Allele Identifier: CA415257497

Gene: EMD

Linked Data

• ClinVar Variation Id: 2886386
• ClinVar RCV Id: RCV003638410
• gnomAD v4: X-154379759-C-G
• MyVariant Identifiers: chrX:g.153608119C>G (hg19) ; chrX:g.154379759C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154379759C>G , CM000685.2:g.154379759C>G	GRCh38
NC_000023.10:g.153608119C>G , CM000685.1:g.153608119C>G	GRCh37
NC_000023.9:g.153261313C>G	NCBI36
NG_008677.1:g.10324C>G , LRG_745:g.10324C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682114.1:c.152C>G	ENSP00000507245.1:p.Pro51Arg
ENST00000682478.1:n.128C>G
ENST00000683576.1:n.128C>G
ENST00000683627.1:c.152C>G	ENSP00000507533.1:p.Pro51Arg
ENST00000684082.1:c.152C>G	ENSP00000508266.1:p.Pro51Arg
ENST00000684633.1:n.124C>G
ENST00000684678.1:c.148C>G	ENSP00000507059.1:p.Pro50Ala
ENST00000369842.9:c.152C>G MANE Select	ENSP00000358857.4:p.Pro51Arg
ENST00000369835.3:c.83-183C>G	ENSP00000358850.3:n.83-183C>G
ENST00000369842.8:c.152C>G	ENSP00000358857.4:p.Pro51Arg
ENST00000428228.5:c.*57C>G	ENSP00000401081.1:n.*57C>G
ENST00000468294.5:n.112C>G
ENST00000485261.1:n.164-183C>G
ENST00000486738.5:n.296C>G
ENST00000492448.1:n.135C>G
ENST00000494443.5:n.209C>G
NM_000117.2:c.152C>G , LRG_745t1:c.152C>G	NP_000108.1:p.Pro51Arg
XM_024452349.1:c.-57C>G	XP_024308117.1:n.-57C>G
NM_000117.3:c.152C>G MANE Select	NP_000108.1:p.Pro51Arg