Canonical Allele Identifier: CA2466663845

Gene: EMD

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154379741G= , CM000685.2:g.154379741G=	GRCh38
NC_000023.10:g.153608101G= , CM000685.1:g.153608101G=	GRCh37
NC_000023.9:g.153261295G=	NCBI36
NG_008677.1:g.10306G= , LRG_745:g.10306G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000682114.1:c.134G=	ENSP00000507245.1:p.Arg45=
ENST00000682478.1:n.110G=
ENST00000683576.1:n.110G=
ENST00000683627.1:c.134G=	ENSP00000507533.1:p.Arg45=
ENST00000684082.1:c.134G=	ENSP00000508266.1:p.Arg45=
ENST00000684633.1:n.106G=
ENST00000684678.1:c.130G=	ENSP00000507059.1:p.Gly44=
ENST00000369842.9:c.134G= MANE Select	ENSP00000358857.4:p.Arg45=
ENST00000369835.3:c.82+175G=	ENSP00000358850.3:n.82+175G=
ENST00000369842.8:c.134G=	ENSP00000358857.4:p.Arg45=
ENST00000428228.5:c.*39G=	ENSP00000401081.1:n.*39G=
ENST00000468294.5:n.94G=
ENST00000485261.1:n.163+175G=
ENST00000486738.5:n.278G=
ENST00000492448.1:n.117G=
ENST00000494443.5:n.191G=
NM_000117.2:c.134G= , LRG_745t1:c.134G=	NP_000108.1:p.Arg45=
XM_024452349.1:c.-75G=	XP_024308117.1:n.-75G=
NM_000117.3:c.134G= MANE Select	NP_000108.1:p.Arg45=