Canonical Allele Identifier: CA2466663678

Gene: EMD

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154379409T= , CM000685.2:g.154379409T=	GRCh38
NC_000023.10:g.153607769T= , CM000685.1:g.153607769T=	GRCh37
NC_000023.9:g.153260963T=	NCBI36
NG_008677.1:g.9974T= , LRG_745:g.9974T=
NG_011506.1:g.238A=
NG_011506.2:g.230A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000369842.9:c.-76T= MANE Select	ENSP00000358857.4:n.-76T=
ENST00000369835.3:c.-76T=	ENSP00000358850.3:n.-76T=
ENST00000369842.8:c.-76T=	ENSP00000358857.4:n.-76T=
ENST00000428228.5:c.-76T=	ENSP00000401081.1:n.-76T=
ENST00000485261.1:n.6T=
ENST00000486738.5:n.69T=
NM_000117.2:c.-76T= , LRG_745t1:c.-76T=	NP_000108.1:n.-76T=
XM_024452349.1:c.-284T=	XP_024308117.1:n.-284T=
NM_000117.3:c.-76T= MANE Select	NP_000108.1:n.-76T=