Canonical Allele Identifier: CA2466663709

Gene: EMD

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154379466G= , CM000685.2:g.154379466G=	GRCh38
NC_000023.10:g.153607826G= , CM000685.1:g.153607826G=	GRCh37
NC_000023.9:g.153261020G=	NCBI36
NG_008677.1:g.10031G= , LRG_745:g.10031G=
NG_011506.1:g.181C=
NG_011506.2:g.173C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682114.1:c.-19G=	ENSP00000507245.1:n.-19G=
ENST00000369842.9:c.-19G= MANE Select	ENSP00000358857.4:n.-19G=
ENST00000369835.3:c.-19G=	ENSP00000358850.3:n.-19G=
ENST00000369842.8:c.-19G=	ENSP00000358857.4:n.-19G=
ENST00000428228.5:c.-19G=	ENSP00000401081.1:n.-19G=
ENST00000485261.1:n.63G=
ENST00000486738.5:n.126G=
ENST00000494443.5:n.39G=
NM_000117.2:c.-19G= , LRG_745t1:c.-19G=	NP_000108.1:n.-19G=
XM_024452349.1:c.-227G=	XP_024308117.1:n.-227G=
NM_000117.3:c.-19G= MANE Select	NP_000108.1:n.-19G=