Canonical Allele Identifier: CA2466664309
Gene: EMD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154380786G= , CM000685.2:g.154380786G= GRCh38
NC_000023.10:g.153609146G= , CM000685.1:g.153609146G= GRCh37
NC_000023.9:g.153262340G= NCBI36
NG_008677.1:g.11351G= , LRG_745:g.11351G=

Transcript Alleles

HGVS Amino-acid change
ENST00000682114.1:c.433G= ENSP00000507245.1:p.Glu145=
ENST00000682478.1:n.623G=
ENST00000683576.1:n.623G=
ENST00000683627.1:c.433G= ENSP00000507533.1:p.Glu145=
ENST00000684082.1:c.390G= ENSP00000508266.1:n.390G=
ENST00000684633.1:n.405G=
ENST00000684678.1:c.429G= ENSP00000507059.1:n.429G=
ENST00000369842.9:c.433G= MANE Select ENSP00000358857.4:p.Glu145=
ENST00000369835.3:c.328G= ENSP00000358850.3:p.Glu110=
ENST00000369842.8:c.433G= ENSP00000358857.4:p.Glu145=
ENST00000428228.5:c.*338G= ENSP00000401081.1:n.*338G=
ENST00000468294.5:n.393G=
ENST00000471965.1:n.222G=
ENST00000485261.1:n.623G=
ENST00000486738.5:n.791G=
ENST00000492448.1:n.416G=
NM_000117.2:c.433G= , LRG_745t1:c.433G= NP_000108.1:p.Glu145=
XM_024452349.1:c.439G= XP_024308117.1:p.Glu147=
NM_000117.3:c.433G= MANE Select NP_000108.1:p.Glu145=