Canonical Allele Identifier: CA2466663680
Gene: EMD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154379414G= , CM000685.2:g.154379414G= GRCh38
NC_000023.10:g.153607774G= , CM000685.1:g.153607774G= GRCh37
NC_000023.9:g.153260968G= NCBI36
NG_008677.1:g.9979G= , LRG_745:g.9979G=
NG_011506.1:g.233C=
NG_011506.2:g.225C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369842.9:c.-71G= MANE Select ENSP00000358857.4:n.-71G=
ENST00000369835.3:c.-71G= ENSP00000358850.3:n.-71G=
ENST00000369842.8:c.-71G= ENSP00000358857.4:n.-71G=
ENST00000428228.5:c.-71G= ENSP00000401081.1:n.-71G=
ENST00000485261.1:n.11G=
ENST00000486738.5:n.74G=
NM_000117.2:c.-71G= , LRG_745t1:c.-71G= NP_000108.1:n.-71G=
XM_024452349.1:c.-279G= XP_024308117.1:n.-279G=
NM_000117.3:c.-71G= MANE Select NP_000108.1:n.-71G=