Canonical Allele Identifier: CA2466663712
Gene: EMD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154379473C= , CM000685.2:g.154379473C= GRCh38
NC_000023.10:g.153607833C= , CM000685.1:g.153607833C= GRCh37
NC_000023.9:g.153261027C= NCBI36
NG_008677.1:g.10038C= , LRG_745:g.10038C=
NG_011506.1:g.174G=
NG_011506.2:g.166G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682114.1:c.-12C= ENSP00000507245.1:n.-12C=
ENST00000369842.9:c.-12C= MANE Select ENSP00000358857.4:n.-12C=
ENST00000369835.3:c.-12C= ENSP00000358850.3:n.-12C=
ENST00000369842.8:c.-12C= ENSP00000358857.4:n.-12C=
ENST00000428228.5:c.-12C= ENSP00000401081.1:n.-12C=
ENST00000485261.1:n.70C=
ENST00000486738.5:n.133C=
ENST00000494443.5:n.46C=
NM_000117.2:c.-12C= , LRG_745t1:c.-12C= NP_000108.1:n.-12C=
XM_024452349.1:c.-220C= XP_024308117.1:n.-220C=
NM_000117.3:c.-12C= MANE Select NP_000108.1:n.-12C=