Canonical Allele Identifier: CA2466664329

Gene: EMD

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154380822A= , CM000685.2:g.154380822A=	GRCh38
NC_000023.10:g.153609182A= , CM000685.1:g.153609182A=	GRCh37
NC_000023.9:g.153262376A=	NCBI36
NG_008677.1:g.11387A= , LRG_745:g.11387A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000682114.1:c.449+20A=	ENSP00000507245.1:n.449+20A=
ENST00000682478.1:n.639+20A=
ENST00000683576.1:n.639+20A=
ENST00000683627.1:c.449+20A=	ENSP00000507533.1:n.449+20A=
ENST00000684082.1:c.406+20A=	ENSP00000508266.1:n.406+20A=
ENST00000684633.1:n.421+20A=
ENST00000684678.1:c.445+20A=	ENSP00000507059.1:n.445+20A=
ENST00000369842.9:c.449+20A= MANE Select	ENSP00000358857.4:n.449+20A=
ENST00000369835.3:c.344+20A=	ENSP00000358850.3:n.344+20A=
ENST00000369842.8:c.449+20A=	ENSP00000358857.4:n.449+20A=
ENST00000428228.5:c.*354+20A=	ENSP00000401081.1:n.*354+20A=
ENST00000468294.5:n.429A=
ENST00000471965.1:n.238+20A=
ENST00000485261.1:n.659A=
ENST00000486738.5:n.827A=
ENST00000492448.1:n.432+20A=
NM_000117.2:c.449+20A= , LRG_745t1:c.449+20A=	NP_000108.1:n.449+20A=
XM_024452349.1:c.455+20A=	XP_024308117.1:n.455+20A=
NM_000117.3:c.449+20A= MANE Select	NP_000108.1:n.449+20A=