Canonical Allele Identifier: CA2466663629

Gene: EMD

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154379318A= , CM000685.2:g.154379318A=	GRCh38
NC_000023.10:g.153607678A= , CM000685.1:g.153607678A=	GRCh37
NC_000023.9:g.153260872A=	NCBI36
NG_008677.1:g.9883A= , LRG_745:g.9883A=
NG_011506.1:g.329T=
NG_011506.2:g.321T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369842.9:c.-167A= MANE Select	ENSP00000358857.4:n.-167A=
ENST00000369835.3:c.-167A=	ENSP00000358850.3:n.-167A=
ENST00000369842.8:c.-167A=	ENSP00000358857.4:n.-167A=
NM_000117.2:c.-167A= , LRG_745t1:c.-167A=	NP_000108.1:n.-167A=
XM_024452349.1:c.-375A=	XP_024308117.1:n.-375A=
NM_000117.3:c.-167A= MANE Select	NP_000108.1:n.-167A=