Canonical Allele Identifier: CA2466664298

Gene: EMD

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154380766A= , CM000685.2:g.154380766A=	GRCh38
NC_000023.10:g.153609126A= , CM000685.1:g.153609126A=	GRCh37
NC_000023.9:g.153262320A=	NCBI36
NG_008677.1:g.11331A= , LRG_745:g.11331A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682114.1:c.413A=	ENSP00000507245.1:p.Asp138=
ENST00000682478.1:n.603A=
ENST00000683576.1:n.603A=
ENST00000683627.1:c.413A=	ENSP00000507533.1:p.Asp138=
ENST00000684082.1:c.370A=	ENSP00000508266.1:n.370A=
ENST00000684633.1:n.385A=
ENST00000684678.1:c.409A=	ENSP00000507059.1:n.409A=
ENST00000369842.9:c.413A= MANE Select	ENSP00000358857.4:p.Asp138=
ENST00000369835.3:c.308A=	ENSP00000358850.3:p.Asp103=
ENST00000369842.8:c.413A=	ENSP00000358857.4:p.Asp138=
ENST00000428228.5:c.*318A=	ENSP00000401081.1:n.*318A=
ENST00000468294.5:n.373A=
ENST00000471965.1:n.202A=
ENST00000485261.1:n.603A=
ENST00000486738.5:n.771A=
ENST00000492448.1:n.396A=
NM_000117.2:c.413A= , LRG_745t1:c.413A=	NP_000108.1:p.Asp138=
XM_024452349.1:c.419A=	XP_024308117.1:p.Asp140=
NM_000117.3:c.413A= MANE Select	NP_000108.1:p.Asp138=