Canonical Allele Identifier: CA2466664402

Gene: EMD

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154380980C= , CM000685.2:g.154380980C=	GRCh38
NC_000023.10:g.153609340C= , CM000685.1:g.153609340C=	GRCh37
NC_000023.9:g.153262534C=	NCBI36
NG_008677.1:g.11545C= , LRG_745:g.11545C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000682114.1:c.548C=	ENSP00000507245.1:p.Pro183=
ENST00000682478.1:n.738C=
ENST00000683576.1:n.738C=
ENST00000683627.1:c.548C=	ENSP00000507533.1:p.Pro183=
ENST00000684082.1:c.505C=	ENSP00000508266.1:n.505C=
ENST00000684633.1:n.520C=
ENST00000684678.1:c.544C=	ENSP00000507059.1:n.544C=
ENST00000369842.9:c.548C= MANE Select	ENSP00000358857.4:p.Pro183=
ENST00000369835.3:c.443C=	ENSP00000358850.3:p.Pro148=
ENST00000369842.8:c.548C=	ENSP00000358857.4:p.Pro183=
ENST00000428228.5:c.*453C=	ENSP00000401081.1:n.*453C=
ENST00000471965.1:n.337C=
ENST00000486738.5:n.985C=
ENST00000492448.1:n.531C=
NM_000117.2:c.548C= , LRG_745t1:c.548C=	NP_000108.1:p.Pro183=
XM_024452349.1:c.554C=	XP_024308117.1:p.Pro185=
NM_000117.3:c.548C= MANE Select	NP_000108.1:p.Pro183=