Canonical Allele Identifier: CA2466663963

Gene: EMD

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154379991A= , CM000685.2:g.154379991A=	GRCh38
NC_000023.10:g.153608351A= , CM000685.1:g.153608351A=	GRCh37
NC_000023.9:g.153261545A=	NCBI36
NG_008677.1:g.10556A= , LRG_745:g.10556A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682114.1:c.237A=	ENSP00000507245.1:p.Lys79=
ENST00000682478.1:n.213A=
ENST00000683576.1:n.213A=
ENST00000683627.1:c.237A=	ENSP00000507533.1:p.Lys79=
ENST00000684082.1:c.237A=	ENSP00000508266.1:p.Lys79=
ENST00000684633.1:n.209A=
ENST00000684678.1:c.233A=	ENSP00000507059.1:n.233A=
ENST00000369842.9:c.237A= MANE Select	ENSP00000358857.4:p.Lys79=
ENST00000369835.3:c.132A=	ENSP00000358850.3:p.Lys44=
ENST00000369842.8:c.237A=	ENSP00000358857.4:p.Lys79=
ENST00000428228.5:c.*142A=	ENSP00000401081.1:n.*142A=
ENST00000468294.5:n.197A=
ENST00000485261.1:n.213A=
ENST00000486738.5:n.381A=
ENST00000492448.1:n.220A=
ENST00000494443.5:n.294A=
NM_000117.2:c.237A= , LRG_745t1:c.237A=	NP_000108.1:p.Lys79=
XM_024452349.1:c.29A=	XP_024308117.1:p.Lys10=
NM_000117.3:c.237A= MANE Select	NP_000108.1:p.Lys79=