Canonical Allele Identifier: CA2466664357

Gene: EMD

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154380889C= , CM000685.2:g.154380889C=	GRCh38
NC_000023.10:g.153609249C= , CM000685.1:g.153609249C=	GRCh37
NC_000023.9:g.153262443C=	NCBI36
NG_008677.1:g.11454C= , LRG_745:g.11454C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000682114.1:c.457C=	ENSP00000507245.1:p.Pro153=
ENST00000682478.1:n.647C=
ENST00000683576.1:n.647C=
ENST00000683627.1:c.457C=	ENSP00000507533.1:p.Pro153=
ENST00000684082.1:c.414C=	ENSP00000508266.1:n.414C=
ENST00000684633.1:n.429C=
ENST00000684678.1:c.453C=	ENSP00000507059.1:n.453C=
ENST00000369842.9:c.457C= MANE Select	ENSP00000358857.4:p.Pro153=
ENST00000369835.3:c.352C=	ENSP00000358850.3:p.Pro118=
ENST00000369842.8:c.457C=	ENSP00000358857.4:p.Pro153=
ENST00000428228.5:c.*362C=	ENSP00000401081.1:n.*362C=
ENST00000468294.5:n.496C=
ENST00000471965.1:n.246C=
ENST00000485261.1:n.726C=
ENST00000486738.5:n.894C=
ENST00000492448.1:n.440C=
NM_000117.2:c.457C= , LRG_745t1:c.457C=	NP_000108.1:p.Pro153=
XM_024452349.1:c.463C=	XP_024308117.1:p.Pro155=
NM_000117.3:c.457C= MANE Select	NP_000108.1:p.Pro153=