Canonical Allele Identifier: CA2466663679

Gene: EMD

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154379411C= , CM000685.2:g.154379411C=	GRCh38
NC_000023.10:g.153607771C= , CM000685.1:g.153607771C=	GRCh37
NC_000023.9:g.153260965C=	NCBI36
NG_008677.1:g.9976C= , LRG_745:g.9976C=
NG_011506.1:g.236G=
NG_011506.2:g.228G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369842.9:c.-74C= MANE Select	ENSP00000358857.4:n.-74C=
ENST00000369835.3:c.-74C=	ENSP00000358850.3:n.-74C=
ENST00000369842.8:c.-74C=	ENSP00000358857.4:n.-74C=
ENST00000428228.5:c.-74C=	ENSP00000401081.1:n.-74C=
ENST00000485261.1:n.8C=
ENST00000486738.5:n.71C=
NM_000117.2:c.-74C= , LRG_745t1:c.-74C=	NP_000108.1:n.-74C=
XM_024452349.1:c.-282C=	XP_024308117.1:n.-282C=
NM_000117.3:c.-74C= MANE Select	NP_000108.1:n.-74C=