Canonical Allele Identifier: CA2466663955

Gene: EMD

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154379960G= , CM000685.2:g.154379960G=	GRCh38
NC_000023.10:g.153608320G= , CM000685.1:g.153608320G=	GRCh37
NC_000023.9:g.153261514G=	NCBI36
NG_008677.1:g.10525G= , LRG_745:g.10525G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682114.1:c.206G=	ENSP00000507245.1:p.Gly69=
ENST00000682478.1:n.182G=
ENST00000683576.1:n.182G=
ENST00000683627.1:c.206G=	ENSP00000507533.1:p.Gly69=
ENST00000684082.1:c.206G=	ENSP00000508266.1:p.Gly69=
ENST00000684633.1:n.178G=
ENST00000684678.1:c.202G=	ENSP00000507059.1:n.202G=
ENST00000369842.9:c.206G= MANE Select	ENSP00000358857.4:p.Gly69=
ENST00000369835.3:c.101G=	ENSP00000358850.3:p.Gly34=
ENST00000369842.8:c.206G=	ENSP00000358857.4:p.Gly69=
ENST00000428228.5:c.*111G=	ENSP00000401081.1:n.*111G=
ENST00000468294.5:n.166G=
ENST00000485261.1:n.182G=
ENST00000486738.5:n.350G=
ENST00000492448.1:n.189G=
ENST00000494443.5:n.263G=
NM_000117.2:c.206G= , LRG_745t1:c.206G=	NP_000108.1:p.Gly69=
XM_024452349.1:c.-3G=	XP_024308117.1:n.-3G=
NM_000117.3:c.206G= MANE Select	NP_000108.1:p.Gly69=