Canonical Allele Identifier: CA2466664032
Gene: EMD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154380155A= , CM000685.2:g.154380155A= GRCh38
NC_000023.10:g.153608515A= , CM000685.1:g.153608515A= GRCh37
NC_000023.9:g.153261709A= NCBI36
NG_008677.1:g.10720A= , LRG_745:g.10720A=

Transcript Alleles

HGVS Amino-acid change
ENST00000682114.1:c.266-79A= ENSP00000507245.1:n.266-79A=
ENST00000682478.1:n.377A=
ENST00000683576.1:n.377A=
ENST00000683627.1:c.266-79A= ENSP00000507533.1:n.266-79A=
ENST00000684082.1:c.266-122A= ENSP00000508266.1:n.266-122A=
ENST00000684633.1:n.238-79A=
ENST00000684678.1:c.262-79A= ENSP00000507059.1:n.262-79A=
ENST00000369842.9:c.266-79A= MANE Select ENSP00000358857.4:n.266-79A=
ENST00000369835.3:c.161-79A= ENSP00000358850.3:n.161-79A=
ENST00000369842.8:c.266-79A= ENSP00000358857.4:n.266-79A=
ENST00000428228.5:c.*171-79A= ENSP00000401081.1:n.*171-79A=
ENST00000468294.5:n.226-79A=
ENST00000485261.1:n.377A=
ENST00000486738.5:n.545A=
ENST00000492448.1:n.249-79A=
ENST00000494443.5:n.458A=
NM_000117.2:c.266-79A= , LRG_745t1:c.266-79A= NP_000108.1:n.266-79A=
XM_024452349.1:c.193A= XP_024308117.1:p.Asn65=
NM_000117.3:c.266-79A= MANE Select NP_000108.1:n.266-79A=