Canonical Allele Identifier: CA2466663748
Gene: EMD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154379558C= , CM000685.2:g.154379558C= GRCh38
NC_000023.10:g.153607918C= , CM000685.1:g.153607918C= GRCh37
NC_000023.9:g.153261112C= NCBI36
NG_008677.1:g.10123C= , LRG_745:g.10123C=
NG_011506.1:g.89G=
NG_011506.2:g.81G=

Transcript Alleles

HGVS Amino-acid change
ENST00000682114.1:c.74C= ENSP00000507245.1:p.Pro25=
ENST00000682478.1:n.50C=
ENST00000683576.1:n.50C=
ENST00000683627.1:c.74C= ENSP00000507533.1:p.Pro25=
ENST00000684082.1:c.74C= ENSP00000508266.1:p.Pro25=
ENST00000684633.1:n.50C=
ENST00000684678.1:c.74C= ENSP00000507059.1:p.Pro25=
ENST00000369842.9:c.74C= MANE Select ENSP00000358857.4:p.Pro25=
ENST00000369835.3:c.74C= ENSP00000358850.3:p.Pro25=
ENST00000369842.8:c.74C= ENSP00000358857.4:p.Pro25=
ENST00000428228.5:c.53+21C= ENSP00000401081.1:n.53+21C=
ENST00000468294.5:n.34C=
ENST00000485261.1:n.155C=
ENST00000486738.5:n.218C=
ENST00000494443.5:n.131C=
NM_000117.2:c.74C= , LRG_745t1:c.74C= NP_000108.1:p.Pro25=
XM_024452349.1:c.-135C= XP_024308117.1:n.-135C=
NM_000117.3:c.74C= MANE Select NP_000108.1:p.Pro25=