Canonical Allele Identifier: CA2466663844
Gene: EMD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154379740A= , CM000685.2:g.154379740A= GRCh38
NC_000023.10:g.153608100A= , CM000685.1:g.153608100A= GRCh37
NC_000023.9:g.153261294A= NCBI36
NG_008677.1:g.10305A= , LRG_745:g.10305A=

Transcript Alleles

HGVS Amino-acid change
ENST00000682114.1:c.133A= ENSP00000507245.1:p.Arg45=
ENST00000682478.1:n.109A=
ENST00000683576.1:n.109A=
ENST00000683627.1:c.133A= ENSP00000507533.1:p.Arg45=
ENST00000684082.1:c.133A= ENSP00000508266.1:p.Arg45=
ENST00000684633.1:n.105A=
ENST00000684678.1:c.129A= ENSP00000507059.1:p.Arg43=
ENST00000369842.9:c.133A= MANE Select ENSP00000358857.4:p.Arg45=
ENST00000369835.3:c.82+174A= ENSP00000358850.3:n.82+174A=
ENST00000369842.8:c.133A= ENSP00000358857.4:p.Arg45=
ENST00000428228.5:c.*38A= ENSP00000401081.1:n.*38A=
ENST00000468294.5:n.93A=
ENST00000485261.1:n.163+174A=
ENST00000486738.5:n.277A=
ENST00000492448.1:n.116A=
ENST00000494443.5:n.190A=
NM_000117.2:c.133A= , LRG_745t1:c.133A= NP_000108.1:p.Arg45=
XM_024452349.1:c.-76A= XP_024308117.1:n.-76A=
NM_000117.3:c.133A= MANE Select NP_000108.1:p.Arg45=