Canonical Allele Identifier: CA2466664030
Gene: EMD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154380147G= , CM000685.2:g.154380147G= GRCh38
NC_000023.10:g.153608507G= , CM000685.1:g.153608507G= GRCh37
NC_000023.9:g.153261701G= NCBI36
NG_008677.1:g.10712G= , LRG_745:g.10712G=

Transcript Alleles

HGVS Amino-acid change
ENST00000682114.1:c.266-87G= ENSP00000507245.1:n.266-87G=
ENST00000682478.1:n.369G=
ENST00000683576.1:n.369G=
ENST00000683627.1:c.266-87G= ENSP00000507533.1:n.266-87G=
ENST00000684082.1:c.265+128G= ENSP00000508266.1:n.265+128G=
ENST00000684633.1:n.238-87G=
ENST00000684678.1:c.262-87G= ENSP00000507059.1:n.262-87G=
ENST00000369842.9:c.266-87G= MANE Select ENSP00000358857.4:n.266-87G=
ENST00000369835.3:c.161-87G= ENSP00000358850.3:n.161-87G=
ENST00000369842.8:c.266-87G= ENSP00000358857.4:n.266-87G=
ENST00000428228.5:c.*171-87G= ENSP00000401081.1:n.*171-87G=
ENST00000468294.5:n.226-87G=
ENST00000485261.1:n.369G=
ENST00000486738.5:n.537G=
ENST00000492448.1:n.249-87G=
ENST00000494443.5:n.450G=
NM_000117.2:c.266-87G= , LRG_745t1:c.266-87G= NP_000108.1:n.266-87G=
XM_024452349.1:c.185G= XP_024308117.1:p.Arg62=
NM_000117.3:c.266-87G= MANE Select NP_000108.1:n.266-87G=