Canonical Allele Identifier: CA2466664355

Gene: EMD

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154380886C= , CM000685.2:g.154380886C=	GRCh38
NC_000023.10:g.153609246C= , CM000685.1:g.153609246C=	GRCh37
NC_000023.9:g.153262440C=	NCBI36
NG_008677.1:g.11451C= , LRG_745:g.11451C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000682114.1:c.454C=	ENSP00000507245.1:p.Arg152=
ENST00000682478.1:n.644C=
ENST00000683576.1:n.644C=
ENST00000683627.1:c.454C=	ENSP00000507533.1:p.Arg152=
ENST00000684082.1:c.411C=	ENSP00000508266.1:n.411C=
ENST00000684633.1:n.426C=
ENST00000684678.1:c.450C=	ENSP00000507059.1:n.450C=
ENST00000369842.9:c.454C= MANE Select	ENSP00000358857.4:p.Arg152=
ENST00000369835.3:c.349C=	ENSP00000358850.3:p.Arg117=
ENST00000369842.8:c.454C=	ENSP00000358857.4:p.Arg152=
ENST00000428228.5:c.*359C=	ENSP00000401081.1:n.*359C=
ENST00000468294.5:n.493C=
ENST00000471965.1:n.243C=
ENST00000485261.1:n.723C=
ENST00000486738.5:n.891C=
ENST00000492448.1:n.437C=
NM_000117.2:c.454C= , LRG_745t1:c.454C=	NP_000108.1:p.Arg152=
XM_024452349.1:c.460C=	XP_024308117.1:p.Arg154=
NM_000117.3:c.454C= MANE Select	NP_000108.1:p.Arg152=