Canonical Allele Identifier: CA2466663622

Gene: EMD

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154379308A= , CM000685.2:g.154379308A=	GRCh38
NC_000023.10:g.153607668A= , CM000685.1:g.153607668A=	GRCh37
NC_000023.9:g.153260862A=	NCBI36
NG_008677.1:g.9873A= , LRG_745:g.9873A=
NG_011506.1:g.339T=
NG_011506.2:g.331T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000369842.9:c.-177A= MANE Select	ENSP00000358857.4:n.-177A=
ENST00000369835.3:c.-177A=	ENSP00000358850.3:n.-177A=
ENST00000369842.8:c.-177A=	ENSP00000358857.4:n.-177A=
NM_000117.2:c.-177A= , LRG_745t1:c.-177A=	NP_000108.1:n.-177A=
XM_024452349.1:c.-385A=	XP_024308117.1:n.-385A=
NM_000117.3:c.-177A= MANE Select	NP_000108.1:n.-177A=