Canonical Allele Identifier: CA2466663818
Gene: EMD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154379677C= , CM000685.2:g.154379677C= GRCh38
NC_000023.10:g.153608037C= , CM000685.1:g.153608037C= GRCh37
NC_000023.9:g.153261231C= NCBI36
NG_008677.1:g.10242C= , LRG_745:g.10242C=

Transcript Alleles

HGVS Amino-acid change
ENST00000682114.1:c.83-13C= ENSP00000507245.1:n.83-13C=
ENST00000682478.1:n.59-13C=
ENST00000683576.1:n.59-13C=
ENST00000683627.1:c.83-13C= ENSP00000507533.1:n.83-13C=
ENST00000684082.1:c.83-13C= ENSP00000508266.1:n.83-13C=
ENST00000684633.1:n.55-13C=
ENST00000684678.1:c.79-13C= ENSP00000507059.1:n.79-13C=
ENST00000369842.9:c.83-13C= MANE Select ENSP00000358857.4:n.83-13C=
ENST00000369835.3:c.82+111C= ENSP00000358850.3:n.82+111C=
ENST00000369842.8:c.83-13C= ENSP00000358857.4:n.83-13C=
ENST00000428228.5:c.54-13C= ENSP00000401081.1:n.54-13C=
ENST00000468294.5:n.43-13C=
ENST00000485261.1:n.163+111C=
ENST00000486738.5:n.227-13C=
ENST00000492448.1:n.53C=
ENST00000494443.5:n.140-13C=
NM_000117.2:c.83-13C= , LRG_745t1:c.83-13C= NP_000108.1:n.83-13C=
XM_024452349.1:c.-126-13C= XP_024308117.1:n.-126-13C=
NM_000117.3:c.83-13C= MANE Select NP_000108.1:n.83-13C=