Canonical Allele Identifier: CA2466663731

Gene: EMD

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154379525C= , CM000685.2:g.154379525C=	GRCh38
NC_000023.10:g.153607885C= , CM000685.1:g.153607885C=	GRCh37
NC_000023.9:g.153261079C=	NCBI36
NG_008677.1:g.10090C= , LRG_745:g.10090C=
NG_011506.1:g.122G=
NG_011506.2:g.114G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682114.1:c.41C=	ENSP00000507245.1:p.Thr14=
ENST00000682478.1:n.17C=
ENST00000683576.1:n.17C=
ENST00000683627.1:c.41C=	ENSP00000507533.1:p.Thr14=
ENST00000684082.1:c.41C=	ENSP00000508266.1:p.Thr14=
ENST00000684633.1:n.17C=
ENST00000684678.1:c.41C=	ENSP00000507059.1:p.Thr14=
ENST00000369842.9:c.41C= MANE Select	ENSP00000358857.4:p.Thr14=
ENST00000369835.3:c.41C=	ENSP00000358850.3:p.Thr14=
ENST00000369842.8:c.41C=	ENSP00000358857.4:p.Thr14=
ENST00000428228.5:c.41C=	ENSP00000401081.1:p.Thr14=
ENST00000468294.5:n.1C=
ENST00000485261.1:n.122C=
ENST00000486738.5:n.185C=
ENST00000494443.5:n.98C=
NM_000117.2:c.41C= , LRG_745t1:c.41C=	NP_000108.1:p.Thr14=
XM_024452349.1:c.-168C=	XP_024308117.1:n.-168C=
NM_000117.3:c.41C= MANE Select	NP_000108.1:p.Thr14=