Canonical Allele Identifier: CA2466663848
Gene: EMD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154379751C= , CM000685.2:g.154379751C= GRCh38
NC_000023.10:g.153608111C= , CM000685.1:g.153608111C= GRCh37
NC_000023.9:g.153261305C= NCBI36
NG_008677.1:g.10316C= , LRG_745:g.10316C=

Transcript Alleles

HGVS Amino-acid change
ENST00000682114.1:c.144C= ENSP00000507245.1:p.Leu48=
ENST00000682478.1:n.120C=
ENST00000683576.1:n.120C=
ENST00000683627.1:c.144C= ENSP00000507533.1:p.Leu48=
ENST00000684082.1:c.144C= ENSP00000508266.1:p.Leu48=
ENST00000684633.1:n.116C=
ENST00000684678.1:c.140C= ENSP00000507059.1:p.Ser47=
ENST00000369842.9:c.144C= MANE Select ENSP00000358857.4:p.Leu48=
ENST00000369835.3:c.82+185C= ENSP00000358850.3:n.82+185C=
ENST00000369842.8:c.144C= ENSP00000358857.4:p.Leu48=
ENST00000428228.5:c.*49C= ENSP00000401081.1:n.*49C=
ENST00000468294.5:n.104C=
ENST00000485261.1:n.163+185C=
ENST00000486738.5:n.288C=
ENST00000492448.1:n.127C=
ENST00000494443.5:n.201C=
NM_000117.2:c.144C= , LRG_745t1:c.144C= NP_000108.1:p.Leu48=
XM_024452349.1:c.-65C= XP_024308117.1:n.-65C=
NM_000117.3:c.144C= MANE Select NP_000108.1:p.Leu48=