Canonical Allele Identifier: CA2466663688

Gene: EMD

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154379437T= , CM000685.2:g.154379437T=	GRCh38
NC_000023.10:g.153607797T= , CM000685.1:g.153607797T=	GRCh37
NC_000023.9:g.153260991T=	NCBI36
NG_008677.1:g.10002T= , LRG_745:g.10002T=
NG_011506.1:g.210A=
NG_011506.2:g.202A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682114.1:c.-48T=	ENSP00000507245.1:n.-48T=
ENST00000369842.9:c.-48T= MANE Select	ENSP00000358857.4:n.-48T=
ENST00000369835.3:c.-48T=	ENSP00000358850.3:n.-48T=
ENST00000369842.8:c.-48T=	ENSP00000358857.4:n.-48T=
ENST00000428228.5:c.-48T=	ENSP00000401081.1:n.-48T=
ENST00000485261.1:n.34T=
ENST00000486738.5:n.97T=
ENST00000494443.5:n.10T=
NM_000117.2:c.-48T= , LRG_745t1:c.-48T=	NP_000108.1:n.-48T=
XM_024452349.1:c.-256T=	XP_024308117.1:n.-256T=
NM_000117.3:c.-48T= MANE Select	NP_000108.1:n.-48T=