Canonical Allele Identifier: CA2466664036
Gene: EMD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154380173G= , CM000685.2:g.154380173G= GRCh38
NC_000023.10:g.153608533G= , CM000685.1:g.153608533G= GRCh37
NC_000023.9:g.153261727G= NCBI36
NG_008677.1:g.10738G= , LRG_745:g.10738G=

Transcript Alleles

HGVS Amino-acid change
ENST00000682114.1:c.266-61G= ENSP00000507245.1:n.266-61G=
ENST00000682478.1:n.395G=
ENST00000683576.1:n.395G=
ENST00000683627.1:c.266-61G= ENSP00000507533.1:n.266-61G=
ENST00000684082.1:c.266-104G= ENSP00000508266.1:n.266-104G=
ENST00000684633.1:n.238-61G=
ENST00000684678.1:c.262-61G= ENSP00000507059.1:n.262-61G=
ENST00000369842.9:c.266-61G= MANE Select ENSP00000358857.4:n.266-61G=
ENST00000369835.3:c.161-61G= ENSP00000358850.3:n.161-61G=
ENST00000369842.8:c.266-61G= ENSP00000358857.4:n.266-61G=
ENST00000428228.5:c.*171-61G= ENSP00000401081.1:n.*171-61G=
ENST00000468294.5:n.226-61G=
ENST00000485261.1:n.395G=
ENST00000486738.5:n.563G=
ENST00000492448.1:n.249-61G=
ENST00000494443.5:n.476G=
NM_000117.2:c.266-61G= , LRG_745t1:c.266-61G= NP_000108.1:n.266-61G=
XM_024452349.1:c.211G= XP_024308117.1:p.Ala71=
NM_000117.3:c.266-61G= MANE Select NP_000108.1:n.266-61G=