Canonical Allele Identifier: CA2466664297

Gene: EMD

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154380765G= , CM000685.2:g.154380765G=	GRCh38
NC_000023.10:g.153609125G= , CM000685.1:g.153609125G=	GRCh37
NC_000023.9:g.153262319G=	NCBI36
NG_008677.1:g.11330G= , LRG_745:g.11330G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682114.1:c.412G=	ENSP00000507245.1:p.Asp138=
ENST00000682478.1:n.602G=
ENST00000683576.1:n.602G=
ENST00000683627.1:c.412G=	ENSP00000507533.1:p.Asp138=
ENST00000684082.1:c.369G=	ENSP00000508266.1:n.369G=
ENST00000684633.1:n.384G=
ENST00000684678.1:c.408G=	ENSP00000507059.1:n.408G=
ENST00000369842.9:c.412G= MANE Select	ENSP00000358857.4:p.Asp138=
ENST00000369835.3:c.307G=	ENSP00000358850.3:p.Asp103=
ENST00000369842.8:c.412G=	ENSP00000358857.4:p.Asp138=
ENST00000428228.5:c.*317G=	ENSP00000401081.1:n.*317G=
ENST00000468294.5:n.372G=
ENST00000471965.1:n.201G=
ENST00000485261.1:n.602G=
ENST00000486738.5:n.770G=
ENST00000492448.1:n.395G=
NM_000117.2:c.412G= , LRG_745t1:c.412G=	NP_000108.1:p.Asp138=
XM_024452349.1:c.418G=	XP_024308117.1:p.Asp140=
NM_000117.3:c.412G= MANE Select	NP_000108.1:p.Asp138=