Canonical Allele Identifier: CA2466663618

Gene: EMD

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154379297C= , CM000685.2:g.154379297C=	GRCh38
NC_000023.10:g.153607657C= , CM000685.1:g.153607657C=	GRCh37
NC_000023.9:g.153260851C=	NCBI36
NG_008677.1:g.9862C= , LRG_745:g.9862C=
NG_011506.1:g.350G=
NG_011506.2:g.342G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369842.9:c.-188C= MANE Select	ENSP00000358857.4:n.-188C=
ENST00000369835.3:c.-188C=	ENSP00000358850.3:n.-188C=
ENST00000369842.8:c.-188C=	ENSP00000358857.4:n.-188C=
NM_000117.2:c.-188C= , LRG_745t1:c.-188C=	NP_000108.1:n.-188C=
XM_024452349.1:c.-396C=	XP_024308117.1:n.-396C=
NM_000117.3:c.-188C= MANE Select	NP_000108.1:n.-188C=