Canonical Allele Identifier: CA2466664316
Gene: EMD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154380802G= , CM000685.2:g.154380802G= GRCh38
NC_000023.10:g.153609162G= , CM000685.1:g.153609162G= GRCh37
NC_000023.9:g.153262356G= NCBI36
NG_008677.1:g.11367G= , LRG_745:g.11367G=

Transcript Alleles

HGVS Amino-acid change
ENST00000682114.1:c.449G= ENSP00000507245.1:p.Arg150=
ENST00000682478.1:n.639G=
ENST00000683576.1:n.639G=
ENST00000683627.1:c.449G= ENSP00000507533.1:p.Arg150=
ENST00000684082.1:c.406G= ENSP00000508266.1:n.406G=
ENST00000684633.1:n.421G=
ENST00000684678.1:c.445G= ENSP00000507059.1:n.445G=
ENST00000369842.9:c.449G= MANE Select ENSP00000358857.4:p.Arg150=
ENST00000369835.3:c.344G= ENSP00000358850.3:p.Arg115=
ENST00000369842.8:c.449G= ENSP00000358857.4:p.Arg150=
ENST00000428228.5:c.*354G= ENSP00000401081.1:n.*354G=
ENST00000468294.5:n.409G=
ENST00000471965.1:n.238G=
ENST00000485261.1:n.639G=
ENST00000486738.5:n.807G=
ENST00000492448.1:n.432G=
NM_000117.2:c.449G= , LRG_745t1:c.449G= NP_000108.1:p.Arg150=
XM_024452349.1:c.455G= XP_024308117.1:p.Arg152=
NM_000117.3:c.449G= MANE Select NP_000108.1:p.Arg150=