Canonical Allele Identifier: CA2466663821
Gene: EMD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154379690G= , CM000685.2:g.154379690G= GRCh38
NC_000023.10:g.153608050G= , CM000685.1:g.153608050G= GRCh37
NC_000023.9:g.153261244G= NCBI36
NG_008677.1:g.10255G= , LRG_745:g.10255G=

Transcript Alleles

HGVS Amino-acid change
ENST00000682114.1:c.83G= ENSP00000507245.1:p.Gly28=
ENST00000682478.1:n.59G=
ENST00000683576.1:n.59G=
ENST00000683627.1:c.83G= ENSP00000507533.1:p.Gly28=
ENST00000684082.1:c.83G= ENSP00000508266.1:p.Gly28=
ENST00000684633.1:n.55G=
ENST00000684678.1:c.79G= ENSP00000507059.1:p.Asp27=
ENST00000369842.9:c.83G= MANE Select ENSP00000358857.4:p.Gly28=
ENST00000369835.3:c.82+124G= ENSP00000358850.3:n.82+124G=
ENST00000369842.8:c.83G= ENSP00000358857.4:p.Gly28=
ENST00000428228.5:c.54G= ENSP00000401081.1:p.Arg18=
ENST00000468294.5:n.43G=
ENST00000485261.1:n.163+124G=
ENST00000486738.5:n.227G=
ENST00000492448.1:n.66G=
ENST00000494443.5:n.140G=
NM_000117.2:c.83G= , LRG_745t1:c.83G= NP_000108.1:p.Gly28=
XM_024452349.1:c.-126G= XP_024308117.1:n.-126G=
NM_000117.3:c.83G= MANE Select NP_000108.1:p.Gly28=