Canonical Allele Identifier: CA2466664400
Gene: EMD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154380979C= , CM000685.2:g.154380979C= GRCh38
NC_000023.10:g.153609339C= , CM000685.1:g.153609339C= GRCh37
NC_000023.9:g.153262533C= NCBI36
NG_008677.1:g.11544C= , LRG_745:g.11544C=

Transcript Alleles

HGVS Amino-acid change
ENST00000682114.1:c.547C= ENSP00000507245.1:p.Pro183=
ENST00000682478.1:n.737C=
ENST00000683576.1:n.737C=
ENST00000683627.1:c.547C= ENSP00000507533.1:p.Pro183=
ENST00000684082.1:c.504C= ENSP00000508266.1:n.504C=
ENST00000684633.1:n.519C=
ENST00000684678.1:c.543C= ENSP00000507059.1:n.543C=
ENST00000369842.9:c.547C= MANE Select ENSP00000358857.4:p.Pro183=
ENST00000369835.3:c.442C= ENSP00000358850.3:p.Pro148=
ENST00000369842.8:c.547C= ENSP00000358857.4:p.Pro183=
ENST00000428228.5:c.*452C= ENSP00000401081.1:n.*452C=
ENST00000471965.1:n.336C=
ENST00000486738.5:n.984C=
ENST00000492448.1:n.530C=
NM_000117.2:c.547C= , LRG_745t1:c.547C= NP_000108.1:p.Pro183=
XM_024452349.1:c.553C= XP_024308117.1:p.Pro185=
NM_000117.3:c.547C= MANE Select NP_000108.1:p.Pro183=