Canonical Allele Identifier: CA2466663716

Gene: EMD

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154379485A= , CM000685.2:g.154379485A=	GRCh38
NC_000023.10:g.153607845A= , CM000685.1:g.153607845A=	GRCh37
NC_000023.9:g.153261039A=	NCBI36
NG_008677.1:g.10050A= , LRG_745:g.10050A=
NG_011506.1:g.162T=
NG_011506.2:g.154T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682114.1:c.1A=	ENSP00000507245.1:p.Met1=
ENST00000683627.1:c.1A=	ENSP00000507533.1:p.Met1=
ENST00000684082.1:c.1A=	ENSP00000508266.1:p.Met1=
ENST00000684678.1:c.1A=	ENSP00000507059.1:p.Met1=
ENST00000369842.9:c.1A= MANE Select	ENSP00000358857.4:p.Met1=
ENST00000369835.3:c.1A=	ENSP00000358850.3:p.Met1=
ENST00000369842.8:c.1A=	ENSP00000358857.4:p.Met1=
ENST00000428228.5:c.1A=	ENSP00000401081.1:p.Met1=
ENST00000485261.1:n.82A=
ENST00000486738.5:n.145A=
ENST00000494443.5:n.58A=
NM_000117.2:c.1A= , LRG_745t1:c.1A=	NP_000108.1:p.Met1=
XM_024452349.1:c.-208A=	XP_024308117.1:n.-208A=
NM_000117.3:c.1A= MANE Select	NP_000108.1:p.Met1=