Canonical Allele Identifier: CA2466664314
Gene: EMD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154380798G= , CM000685.2:g.154380798G= GRCh38
NC_000023.10:g.153609158G= , CM000685.1:g.153609158G= GRCh37
NC_000023.9:g.153262352G= NCBI36
NG_008677.1:g.11363G= , LRG_745:g.11363G=

Transcript Alleles

HGVS Amino-acid change
ENST00000682114.1:c.445G= ENSP00000507245.1:p.Asp149=
ENST00000682478.1:n.635G=
ENST00000683576.1:n.635G=
ENST00000683627.1:c.445G= ENSP00000507533.1:p.Asp149=
ENST00000684082.1:c.402G= ENSP00000508266.1:n.402G=
ENST00000684633.1:n.417G=
ENST00000684678.1:c.441G= ENSP00000507059.1:n.441G=
ENST00000369842.9:c.445G= MANE Select ENSP00000358857.4:p.Asp149=
ENST00000369835.3:c.340G= ENSP00000358850.3:p.Asp114=
ENST00000369842.8:c.445G= ENSP00000358857.4:p.Asp149=
ENST00000428228.5:c.*350G= ENSP00000401081.1:n.*350G=
ENST00000468294.5:n.405G=
ENST00000471965.1:n.234G=
ENST00000485261.1:n.635G=
ENST00000486738.5:n.803G=
ENST00000492448.1:n.428G=
NM_000117.2:c.445G= , LRG_745t1:c.445G= NP_000108.1:p.Asp149=
XM_024452349.1:c.451G= XP_024308117.1:p.Asp151=
NM_000117.3:c.445G= MANE Select NP_000108.1:p.Asp149=