Canonical Allele Identifier: CA415259052

Gene: EMD

Linked Data

• MyVariant Identifiers: chrX:g.153609421A>G (hg19) ; chrX:g.154381061A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154381061A>G , CM000685.2:g.154381061A>G	GRCh38
NC_000023.10:g.153609421A>G , CM000685.1:g.153609421A>G	GRCh37
NC_000023.9:g.153262615A>G	NCBI36
NG_008677.1:g.11626A>G , LRG_745:g.11626A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682114.1:c.572+57A>G	ENSP00000507245.1:n.572+57A>G
ENST00000682478.1:n.762+57A>G
ENST00000683576.1:n.819A>G
ENST00000683627.1:c.629A>G	ENSP00000507533.1:p.Asn210Ser
ENST00000684082.1:c.586A>G	ENSP00000508266.1:n.586A>G
ENST00000684633.1:n.601A>G
ENST00000684678.1:c.568+57A>G	ENSP00000507059.1:n.568+57A>G
ENST00000369842.9:c.629A>G MANE Select	ENSP00000358857.4:p.Asn210Ser
ENST00000369835.3:c.524A>G	ENSP00000358850.3:p.Asn175Ser
ENST00000369842.8:c.629A>G	ENSP00000358857.4:p.Asn210Ser
ENST00000428228.5:c.*534A>G	ENSP00000401081.1:n.*534A>G
ENST00000471965.1:n.418A>G
ENST00000486738.5:n.1066A>G
ENST00000492448.1:n.612A>G
NM_000117.2:c.629A>G , LRG_745t1:c.629A>G	NP_000108.1:p.Asn210Ser
XM_024452349.1:c.635A>G	XP_024308117.1:p.Asn212Ser
NM_000117.3:c.629A>G MANE Select	NP_000108.1:p.Asn210Ser