Canonical Allele Identifier: CA2466664470

Gene: EMD

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154381104G= , CM000685.2:g.154381104G=	GRCh38
NC_000023.10:g.153609464G= , CM000685.1:g.153609464G=	GRCh37
NC_000023.9:g.153262658G=	NCBI36
NG_008677.1:g.11669G= , LRG_745:g.11669G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682114.1:c.572+100G=	ENSP00000507245.1:n.572+100G=
ENST00000682478.1:n.762+100G=
ENST00000683576.1:n.862G=
ENST00000683627.1:c.672G=	ENSP00000507533.1:p.Pro224=
ENST00000684082.1:c.629G=	ENSP00000508266.1:n.629G=
ENST00000684633.1:n.644G=
ENST00000684678.1:c.568+100G=	ENSP00000507059.1:n.568+100G=
ENST00000369842.9:c.672G= MANE Select	ENSP00000358857.4:p.Pro224=
ENST00000369835.3:c.567G=	ENSP00000358850.3:p.Pro189=
ENST00000369842.8:c.672G=	ENSP00000358857.4:p.Pro224=
ENST00000428228.5:c.*577G=	ENSP00000401081.1:n.*577G=
ENST00000471965.1:n.461G=
ENST00000486738.5:n.1109G=
ENST00000492448.1:n.655G=
NM_000117.2:c.672G= , LRG_745t1:c.672G=	NP_000108.1:p.Pro224=
XM_024452349.1:c.678G=	XP_024308117.1:p.Pro226=
NM_000117.3:c.672G= MANE Select	NP_000108.1:p.Pro224=