Canonical Allele Identifier: CA2466663773

Gene: EMD

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154379598C= , CM000685.2:g.154379598C=	GRCh38
NC_000023.10:g.153607958C= , CM000685.1:g.153607958C=	GRCh37
NC_000023.9:g.153261152C=	NCBI36
NG_008677.1:g.10163C= , LRG_745:g.10163C=
NG_011506.1:g.49G=
NG_011506.2:g.41G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000682114.1:c.82+32C=	ENSP00000507245.1:n.82+32C=
ENST00000682478.1:n.58+32C=
ENST00000683576.1:n.58+32C=
ENST00000683627.1:c.82+32C=	ENSP00000507533.1:n.82+32C=
ENST00000684082.1:c.82+32C=	ENSP00000508266.1:n.82+32C=
ENST00000684633.1:n.54+36C=
ENST00000684678.1:c.78+36C=	ENSP00000507059.1:n.78+36C=
ENST00000369842.9:c.82+32C= MANE Select	ENSP00000358857.4:n.82+32C=
ENST00000369835.3:c.82+32C=	ENSP00000358850.3:n.82+32C=
ENST00000369842.8:c.82+32C=	ENSP00000358857.4:n.82+32C=
ENST00000428228.5:c.53+61C=	ENSP00000401081.1:n.53+61C=
ENST00000468294.5:n.42+32C=
ENST00000485261.1:n.163+32C=
ENST00000486738.5:n.226+32C=
ENST00000494443.5:n.139+32C=
NM_000117.2:c.82+32C= , LRG_745t1:c.82+32C=	NP_000108.1:n.82+32C=
XM_024452349.1:c.-127+32C=	XP_024308117.1:n.-127+32C=
NM_000117.3:c.82+32C= MANE Select	NP_000108.1:n.82+32C=