Canonical Allele Identifier: CA2466663689

Gene: EMD

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154379438G= , CM000685.2:g.154379438G=	GRCh38
NC_000023.10:g.153607798G= , CM000685.1:g.153607798G=	GRCh37
NC_000023.9:g.153260992G=	NCBI36
NG_008677.1:g.10003G= , LRG_745:g.10003G=
NG_011506.1:g.209C=
NG_011506.2:g.201C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682114.1:c.-47G=	ENSP00000507245.1:n.-47G=
ENST00000369842.9:c.-47G= MANE Select	ENSP00000358857.4:n.-47G=
ENST00000369835.3:c.-47G=	ENSP00000358850.3:n.-47G=
ENST00000369842.8:c.-47G=	ENSP00000358857.4:n.-47G=
ENST00000428228.5:c.-47G=	ENSP00000401081.1:n.-47G=
ENST00000485261.1:n.35G=
ENST00000486738.5:n.98G=
ENST00000494443.5:n.11G=
NM_000117.2:c.-47G= , LRG_745t1:c.-47G=	NP_000108.1:n.-47G=
XM_024452349.1:c.-255G=	XP_024308117.1:n.-255G=
NM_000117.3:c.-47G= MANE Select	NP_000108.1:n.-47G=