Canonical Allele Identifier: CA2466663721

Gene: EMD

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154379498C= , CM000685.2:g.154379498C=	GRCh38
NC_000023.10:g.153607858C= , CM000685.1:g.153607858C=	GRCh37
NC_000023.9:g.153261052C=	NCBI36
NG_008677.1:g.10063C= , LRG_745:g.10063C=
NG_011506.1:g.149G=
NG_011506.2:g.141G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000682114.1:c.14C=	ENSP00000507245.1:p.Ala5=
ENST00000683627.1:c.14C=	ENSP00000507533.1:p.Ala5=
ENST00000684082.1:c.14C=	ENSP00000508266.1:p.Ala5=
ENST00000684678.1:c.14C=	ENSP00000507059.1:p.Ala5=
ENST00000369842.9:c.14C= MANE Select	ENSP00000358857.4:p.Ala5=
ENST00000369835.3:c.14C=	ENSP00000358850.3:p.Ala5=
ENST00000369842.8:c.14C=	ENSP00000358857.4:p.Ala5=
ENST00000428228.5:c.14C=	ENSP00000401081.1:p.Ala5=
ENST00000485261.1:n.95C=
ENST00000486738.5:n.158C=
ENST00000494443.5:n.71C=
NM_000117.2:c.14C= , LRG_745t1:c.14C=	NP_000108.1:p.Ala5=
XM_024452349.1:c.-195C=	XP_024308117.1:n.-195C=
NM_000117.3:c.14C= MANE Select	NP_000108.1:p.Ala5=