Canonical Allele Identifier: CA2466664404
Gene: EMD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154380983C= , CM000685.2:g.154380983C= GRCh38
NC_000023.10:g.153609343C= , CM000685.1:g.153609343C= GRCh37
NC_000023.9:g.153262537C= NCBI36
NG_008677.1:g.11548C= , LRG_745:g.11548C=

Transcript Alleles

HGVS Amino-acid change
ENST00000682114.1:c.551C= ENSP00000507245.1:p.Thr184=
ENST00000682478.1:n.741C=
ENST00000683576.1:n.741C=
ENST00000683627.1:c.551C= ENSP00000507533.1:p.Thr184=
ENST00000684082.1:c.508C= ENSP00000508266.1:n.508C=
ENST00000684633.1:n.523C=
ENST00000684678.1:c.547C= ENSP00000507059.1:n.547C=
ENST00000369842.9:c.551C= MANE Select ENSP00000358857.4:p.Thr184=
ENST00000369835.3:c.446C= ENSP00000358850.3:p.Thr149=
ENST00000369842.8:c.551C= ENSP00000358857.4:p.Thr184=
ENST00000428228.5:c.*456C= ENSP00000401081.1:n.*456C=
ENST00000471965.1:n.340C=
ENST00000486738.5:n.988C=
ENST00000492448.1:n.534C=
NM_000117.2:c.551C= , LRG_745t1:c.551C= NP_000108.1:p.Thr184=
XM_024452349.1:c.557C= XP_024308117.1:p.Thr186=
NM_000117.3:c.551C= MANE Select NP_000108.1:p.Thr184=