Canonical Allele Identifier: CA2466664321
Gene: EMD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154380811T= , CM000685.2:g.154380811T= GRCh38
NC_000023.10:g.153609171T= , CM000685.1:g.153609171T= GRCh37
NC_000023.9:g.153262365T= NCBI36
NG_008677.1:g.11376T= , LRG_745:g.11376T=

Transcript Alleles

HGVS Amino-acid change
ENST00000682114.1:c.449+9T= ENSP00000507245.1:n.449+9T=
ENST00000682478.1:n.639+9T=
ENST00000683576.1:n.639+9T=
ENST00000683627.1:c.449+9T= ENSP00000507533.1:n.449+9T=
ENST00000684082.1:c.406+9T= ENSP00000508266.1:n.406+9T=
ENST00000684633.1:n.421+9T=
ENST00000684678.1:c.445+9T= ENSP00000507059.1:n.445+9T=
ENST00000369842.9:c.449+9T= MANE Select ENSP00000358857.4:n.449+9T=
ENST00000369835.3:c.344+9T= ENSP00000358850.3:n.344+9T=
ENST00000369842.8:c.449+9T= ENSP00000358857.4:n.449+9T=
ENST00000428228.5:c.*354+9T= ENSP00000401081.1:n.*354+9T=
ENST00000468294.5:n.418T=
ENST00000471965.1:n.238+9T=
ENST00000485261.1:n.648T=
ENST00000486738.5:n.816T=
ENST00000492448.1:n.432+9T=
NM_000117.2:c.449+9T= , LRG_745t1:c.449+9T= NP_000108.1:n.449+9T=
XM_024452349.1:c.455+9T= XP_024308117.1:n.455+9T=
NM_000117.3:c.449+9T= MANE Select NP_000108.1:n.449+9T=