Canonical Allele Identifier: CA2466663697
Gene: EMD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154379447G= , CM000685.2:g.154379447G= GRCh38
NC_000023.10:g.153607807G= , CM000685.1:g.153607807G= GRCh37
NC_000023.9:g.153261001G= NCBI36
NG_008677.1:g.10012G= , LRG_745:g.10012G=
NG_011506.1:g.200C=
NG_011506.2:g.192C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682114.1:c.-38G= ENSP00000507245.1:n.-38G=
ENST00000369842.9:c.-38G= MANE Select ENSP00000358857.4:n.-38G=
ENST00000369835.3:c.-38G= ENSP00000358850.3:n.-38G=
ENST00000369842.8:c.-38G= ENSP00000358857.4:n.-38G=
ENST00000428228.5:c.-38G= ENSP00000401081.1:n.-38G=
ENST00000485261.1:n.44G=
ENST00000486738.5:n.107G=
ENST00000494443.5:n.20G=
NM_000117.2:c.-38G= , LRG_745t1:c.-38G= NP_000108.1:n.-38G=
XM_024452349.1:c.-246G= XP_024308117.1:n.-246G=
NM_000117.3:c.-38G= MANE Select NP_000108.1:n.-38G=