Canonical Allele Identifier: CA2466664406

Gene: EMD

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154380986C= , CM000685.2:g.154380986C=	GRCh38
NC_000023.10:g.153609346C= , CM000685.1:g.153609346C=	GRCh37
NC_000023.9:g.153262540C=	NCBI36
NG_008677.1:g.11551C= , LRG_745:g.11551C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682114.1:c.554C=	ENSP00000507245.1:p.Ser185=
ENST00000682478.1:n.744C=
ENST00000683576.1:n.744C=
ENST00000683627.1:c.554C=	ENSP00000507533.1:p.Ser185=
ENST00000684082.1:c.511C=	ENSP00000508266.1:n.511C=
ENST00000684633.1:n.526C=
ENST00000684678.1:c.550C=	ENSP00000507059.1:n.550C=
ENST00000369842.9:c.554C= MANE Select	ENSP00000358857.4:p.Ser185=
ENST00000369835.3:c.449C=	ENSP00000358850.3:p.Ser150=
ENST00000369842.8:c.554C=	ENSP00000358857.4:p.Ser185=
ENST00000428228.5:c.*459C=	ENSP00000401081.1:n.*459C=
ENST00000471965.1:n.343C=
ENST00000486738.5:n.991C=
ENST00000492448.1:n.537C=
NM_000117.2:c.554C= , LRG_745t1:c.554C=	NP_000108.1:p.Ser185=
XM_024452349.1:c.560C=	XP_024308117.1:p.Ser187=
NM_000117.3:c.554C= MANE Select	NP_000108.1:p.Ser185=