Canonical Allele Identifier: CA2466663850
Gene: EMD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154379755C= , CM000685.2:g.154379755C= GRCh38
NC_000023.10:g.153608115C= , CM000685.1:g.153608115C= GRCh37
NC_000023.9:g.153261309C= NCBI36
NG_008677.1:g.10320C= , LRG_745:g.10320C=

Transcript Alleles

HGVS Amino-acid change
ENST00000682114.1:c.148C= ENSP00000507245.1:p.Pro50=
ENST00000682478.1:n.124C=
ENST00000683576.1:n.124C=
ENST00000683627.1:c.148C= ENSP00000507533.1:p.Pro50=
ENST00000684082.1:c.148C= ENSP00000508266.1:p.Pro50=
ENST00000684633.1:n.120C=
ENST00000684678.1:c.144C= ENSP00000507059.1:p.Arg48=
ENST00000369842.9:c.148C= MANE Select ENSP00000358857.4:p.Pro50=
ENST00000369835.3:c.83-187C= ENSP00000358850.3:n.83-187C=
ENST00000369842.8:c.148C= ENSP00000358857.4:p.Pro50=
ENST00000428228.5:c.*53C= ENSP00000401081.1:n.*53C=
ENST00000468294.5:n.108C=
ENST00000485261.1:n.164-187C=
ENST00000486738.5:n.292C=
ENST00000492448.1:n.131C=
ENST00000494443.5:n.205C=
NM_000117.2:c.148C= , LRG_745t1:c.148C= NP_000108.1:p.Pro50=
XM_024452349.1:c.-61C= XP_024308117.1:n.-61C=
NM_000117.3:c.148C= MANE Select NP_000108.1:p.Pro50=