Canonical Allele Identifier: CA2466664409

Gene: EMD

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154380994A= , CM000685.2:g.154380994A=	GRCh38
NC_000023.10:g.153609354A= , CM000685.1:g.153609354A=	GRCh37
NC_000023.9:g.153262548A=	NCBI36
NG_008677.1:g.11559A= , LRG_745:g.11559A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000682114.1:c.562A=	ENSP00000507245.1:p.Thr188=
ENST00000682478.1:n.752A=
ENST00000683576.1:n.752A=
ENST00000683627.1:c.562A=	ENSP00000507533.1:p.Thr188=
ENST00000684082.1:c.519A=	ENSP00000508266.1:n.519A=
ENST00000684633.1:n.534A=
ENST00000684678.1:c.558A=	ENSP00000507059.1:n.558A=
ENST00000369842.9:c.562A= MANE Select	ENSP00000358857.4:p.Thr188=
ENST00000369835.3:c.457A=	ENSP00000358850.3:p.Thr153=
ENST00000369842.8:c.562A=	ENSP00000358857.4:p.Thr188=
ENST00000428228.5:c.*467A=	ENSP00000401081.1:n.*467A=
ENST00000471965.1:n.351A=
ENST00000486738.5:n.999A=
ENST00000492448.1:n.545A=
NM_000117.2:c.562A= , LRG_745t1:c.562A=	NP_000108.1:p.Thr188=
XM_024452349.1:c.568A=	XP_024308117.1:p.Thr190=
NM_000117.3:c.562A= MANE Select	NP_000108.1:p.Thr188=