Canonical Allele Identifier: CA2466663794
Gene: EMD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154379639C= , CM000685.2:g.154379639C= GRCh38
NC_000023.10:g.153607999C= , CM000685.1:g.153607999C= GRCh37
NC_000023.9:g.153261193C= NCBI36
NG_008677.1:g.10204C= , LRG_745:g.10204C=
NG_011506.1:g.8G=

Transcript Alleles

HGVS Amino-acid change
ENST00000682114.1:c.83-51C= ENSP00000507245.1:n.83-51C=
ENST00000682478.1:n.59-51C=
ENST00000683576.1:n.59-51C=
ENST00000683627.1:c.83-51C= ENSP00000507533.1:n.83-51C=
ENST00000684082.1:c.83-51C= ENSP00000508266.1:n.83-51C=
ENST00000684633.1:n.55-51C=
ENST00000684678.1:c.79-51C= ENSP00000507059.1:n.79-51C=
ENST00000369842.9:c.83-51C= MANE Select ENSP00000358857.4:n.83-51C=
ENST00000369835.3:c.82+73C= ENSP00000358850.3:n.82+73C=
ENST00000369842.8:c.83-51C= ENSP00000358857.4:n.83-51C=
ENST00000428228.5:c.54-51C= ENSP00000401081.1:n.54-51C=
ENST00000468294.5:n.43-51C=
ENST00000485261.1:n.163+73C=
ENST00000486738.5:n.227-51C=
ENST00000492448.1:n.15C=
ENST00000494443.5:n.140-51C=
NM_000117.2:c.83-51C= , LRG_745t1:c.83-51C= NP_000108.1:n.83-51C=
XM_024452349.1:c.-126-51C= XP_024308117.1:n.-126-51C=
NM_000117.3:c.83-51C= MANE Select NP_000108.1:n.83-51C=