Canonical Allele Identifier: CA2466663750
Gene: EMD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154379560G= , CM000685.2:g.154379560G= GRCh38
NC_000023.10:g.153607920G= , CM000685.1:g.153607920G= GRCh37
NC_000023.9:g.153261114G= NCBI36
NG_008677.1:g.10125G= , LRG_745:g.10125G=
NG_011506.1:g.87C=
NG_011506.2:g.79C=

Transcript Alleles

HGVS Amino-acid change
ENST00000682114.1:c.76G= ENSP00000507245.1:p.Val26=
ENST00000682478.1:n.52G=
ENST00000683576.1:n.52G=
ENST00000683627.1:c.76G= ENSP00000507533.1:p.Val26=
ENST00000684082.1:c.76G= ENSP00000508266.1:p.Val26=
ENST00000684633.1:n.52G=
ENST00000684678.1:c.76G= ENSP00000507059.1:p.Val26=
ENST00000369842.9:c.76G= MANE Select ENSP00000358857.4:p.Val26=
ENST00000369835.3:c.76G= ENSP00000358850.3:p.Val26=
ENST00000369842.8:c.76G= ENSP00000358857.4:p.Val26=
ENST00000428228.5:c.53+23G= ENSP00000401081.1:n.53+23G=
ENST00000468294.5:n.36G=
ENST00000485261.1:n.157G=
ENST00000486738.5:n.220G=
ENST00000494443.5:n.133G=
NM_000117.2:c.76G= , LRG_745t1:c.76G= NP_000108.1:p.Val26=
XM_024452349.1:c.-133G= XP_024308117.1:n.-133G=
NM_000117.3:c.76G= MANE Select NP_000108.1:p.Val26=