Canonical Allele Identifier: CA2466663630

Gene: EMD

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154379319C= , CM000685.2:g.154379319C=	GRCh38
NC_000023.10:g.153607679C= , CM000685.1:g.153607679C=	GRCh37
NC_000023.9:g.153260873C=	NCBI36
NG_008677.1:g.9884C= , LRG_745:g.9884C=
NG_011506.1:g.328G=
NG_011506.2:g.320G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000369842.9:c.-166C= MANE Select	ENSP00000358857.4:n.-166C=
ENST00000369835.3:c.-166C=	ENSP00000358850.3:n.-166C=
ENST00000369842.8:c.-166C=	ENSP00000358857.4:n.-166C=
NM_000117.2:c.-166C= , LRG_745t1:c.-166C=	NP_000108.1:n.-166C=
XM_024452349.1:c.-374C=	XP_024308117.1:n.-374C=
NM_000117.3:c.-166C= MANE Select	NP_000108.1:n.-166C=