Canonical Allele Identifier: CA2466663780

Gene: EMD

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154379607C= , CM000685.2:g.154379607C=	GRCh38
NC_000023.10:g.153607967C= , CM000685.1:g.153607967C=	GRCh37
NC_000023.9:g.153261161C=	NCBI36
NG_008677.1:g.10172C= , LRG_745:g.10172C=
NG_011506.1:g.40G=
NG_011506.2:g.32G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000682114.1:c.82+41C=	ENSP00000507245.1:n.82+41C=
ENST00000682478.1:n.58+41C=
ENST00000683576.1:n.58+41C=
ENST00000683627.1:c.82+41C=	ENSP00000507533.1:n.82+41C=
ENST00000684082.1:c.82+41C=	ENSP00000508266.1:n.82+41C=
ENST00000684633.1:n.54+45C=
ENST00000684678.1:c.78+45C=	ENSP00000507059.1:n.78+45C=
ENST00000369842.9:c.82+41C= MANE Select	ENSP00000358857.4:n.82+41C=
ENST00000369835.3:c.82+41C=	ENSP00000358850.3:n.82+41C=
ENST00000369842.8:c.82+41C=	ENSP00000358857.4:n.82+41C=
ENST00000428228.5:c.53+70C=	ENSP00000401081.1:n.53+70C=
ENST00000468294.5:n.42+41C=
ENST00000485261.1:n.163+41C=
ENST00000486738.5:n.226+41C=
ENST00000494443.5:n.139+41C=
NM_000117.2:c.82+41C= , LRG_745t1:c.82+41C=	NP_000108.1:n.82+41C=
XM_024452349.1:c.-127+41C=	XP_024308117.1:n.-127+41C=
NM_000117.3:c.82+41C= MANE Select	NP_000108.1:n.82+41C=