Canonical Allele Identifier: CA415258146

Gene: EMD

Linked Data

• MyVariant Identifiers: chrX:g.153609116C>A (hg19) ; chrX:g.154380756C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154380756C>A , CM000685.2:g.154380756C>A	GRCh38
NC_000023.10:g.153609116C>A , CM000685.1:g.153609116C>A	GRCh37
NC_000023.9:g.153262310C>A	NCBI36
NG_008677.1:g.11321C>A , LRG_745:g.11321C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682114.1:c.403C>A	ENSP00000507245.1:p.His135Asn
ENST00000682478.1:n.593C>A
ENST00000683576.1:n.593C>A
ENST00000683627.1:c.403C>A	ENSP00000507533.1:p.His135Asn
ENST00000684082.1:c.360C>A	ENSP00000508266.1:n.360C>A
ENST00000684633.1:n.375C>A
ENST00000684678.1:c.399C>A	ENSP00000507059.1:n.399C>A
ENST00000369842.9:c.403C>A MANE Select	ENSP00000358857.4:p.His135Asn
ENST00000369835.3:c.298C>A	ENSP00000358850.3:p.His100Asn
ENST00000369842.8:c.403C>A	ENSP00000358857.4:p.His135Asn
ENST00000428228.5:c.*308C>A	ENSP00000401081.1:n.*308C>A
ENST00000468294.5:n.363C>A
ENST00000471965.1:n.192C>A
ENST00000485261.1:n.593C>A
ENST00000486738.5:n.761C>A
ENST00000492448.1:n.386C>A
NM_000117.2:c.403C>A , LRG_745t1:c.403C>A	NP_000108.1:p.His135Asn
XM_024452349.1:c.409C>A	XP_024308117.1:p.His137Asn
NM_000117.3:c.403C>A MANE Select	NP_000108.1:p.His135Asn